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Genetics and Prenatal Development

Why learn about prenatal development and genetics?

People endure quite an incredible journey before they are born. Think about it—when the timing
and conditions are just right, a tiny egg releases from ovulation and a single sperm out of hundreds
of millions unite to begin the process of fertilization. Genetic material from the mother and father
join together to form a completely new organism. This new organism has to continue to travel and
implant in the uterine wall in order to continue to grow and thrive. It is not an easy feat. It still must
grow and develop for approximately 268 days before it begins life outside of the womb.

Today we have more knowledge and technology than ever before that has an impact on this process.
We are privy to tests that can give us a wealth of information even before we conceive. We have the
ability to know the genetic make-up of an embryo before it is implanted in the womb. If you could
choose all of the features of your future baby, would you? What would be the pros and cons of this?
New parents also have the choice of the prenatal care that they receive and how they want to

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prepare for labor and delivery. As you can see, the choices that are made along the way and the
unforeseen surprises make for a unique pregnancy and birth story.

This module explores this journey and the development process from the moment of conception to
delivery.

What you’ll learn to do: explain the role of genetics in prenatal

development

In this section, we will look at some of the ways in which heredity helps to shape the way we are.
Heredity involves more than genetic information from our parents. According to evolutionary
psychology, our genetic inheritance comes from the most adaptive genes of our ancestors. We will
look at what happens genetically during conception and take a brief look at some genetic
abnormalities. Before going into these topics, however, it is important to emphasize the interplay
between heredity and the environment. Why are you the way you are? As you consider some of
your features (height, weight, personality, health, etc.), ask yourself whether these features are a
result of heredity, or environmental factors, or both. Chances are, you can see the ways in which
both heredity and environmental factors (such as lifestyle, diet, and so on) have contributed to these
features.

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Learning outcomes

Explain the evolutionary psychology perspective of lifespan development

Describe genetic components of conception
Describe genes and their importance in genetic inheritance
Describe chromosomal abnormalities
Explain the value of prenatal testing
Describe the interaction between genetics and the environment
Compare monozygotic and dizygotic twins

Evolutionary Psychology

Evolutionary Psychology

Evolutionary
psychology focuses on how
universal patterns of behavior
and cognitive processes have
evolved over time. Variations
in cognition and behavior
would make individuals more
or less successful in
reproducing and passing those
genes to their
offspring. Evolutionary
psychologists study a variety
of psychological phenomena Figure 1. Evolutionary psychology examines the connection between
that may have evolved as biological adaptation and preferences in mate selection.

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adaptations, including the fear response, food preferences, mate selection, and cooperative
behaviors (Confer et al., 2010).

Many think of evolution as the development of traits and behaviors that allow us to survive this
“dog-eat-dog” world, like strong leg muscles to run fast, or fists to punch and defend ourselves.
However, physical survival is only important if it eventually contributes to successful reproduction.
That is, even if you live to be 100 years old if you fail to mate and produce children, your genes will
die with your body. Thus, reproductive success, not survival success, is the engine of evolution by
natural selection.

Charles Darwin describes this process in the theory of evolution by natural selection. In simple
terms, the theory states that organisms that are better suited for their environment will survive and
reproduce, while those that are poorly suited for their environment will die off. There is a growing
interest in applying the principles of evolutionary psychology to better understand lifespan
development in humans.

The Evolutionary Perspective: Genetic Inheritance from our

Ancestors

The fundamentals of the evolutionary perspective

One very influential approach in understanding human development is the evolutionary perspective,
the final developmental perspective that we will consider. This perspective seeks to identify
behavior that is the result of our genetic inheritance from our ancestors. Evolutionary
psychology is a theoretical approach in the social and natural sciences that examines psychological
structure from a modern evolutionary perspective. It seeks to identify which human psychological
traits are evolved adaptations – that is, the functional products of natural selection or sexual
selection in human evolution.
David M. Buss is an evolutionary psychologist at the University of Texas at Austin, theorizing and
researching human sex differences in mate selection. The primary topics of his research include
male mating strategies, conflict between the sexes, social status, social reputation, prestige, the
emotion of jealousy, homicide, anti-homicide defenses, and—most recently—stalking. All of these
are approached from an evolutionary perspective.
Evolutionary psychology has its historical roots in Charles Darwin’s theory of natural
selection. In The Origin of Species, Darwin predicted that psychology would develop an
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evolutionary basis and that a process of natural selection creates traits in

a species that is adaptive to its environment.

Using Darwin’s arguments, evolutionary approaches claim that one’s

genetic inheritance not only determine such physical traits as skin and
eye color, but also certain personality traits and social behaviors. For
example, some evolutionary developmental psychologists suggest that
behavior such as shyness and jealousy may be produced in part by
genetic causes, presumably because they helped increase the survival
rates of human’s ancient relatives. Figure 6. A portrait of
There is a general acceptance that Darwin’s evolutionary theory provides Charles Robert Darwin. In
an accurate description of basic genetic processes and that the the distant future, I see
evolutionary perspective is increasingly visible in the field of lifespan open fields for far more
important researches.
development. However, applications of the evolutionary perspective
Psychology will be
have been subjected to considerable criticism. Some developmental based on a new
psychologists are concerned about too much emphasis on genetic and foundation, that of the
biological aspects of behavior and suggest that the evolutionary necessary acquirement
perspective places insufficient attention on environmental and social of each mental power
factors involved in producing children’s and adults’ behavior. Other and capacity by
critics argue that there is no good way to experimentally test theories gradation. — DARWIN,
derived from this approach because humans evolved so long ago. For CHARLES (1859). THE ORIGIN
example, we may admit that jealousy helps individuals to survive more OF SPECIES . P. 488 –
VIA WIKISOURCE
effectively, but how do we prove it. All things considered, however, the
evolutionary approach is continually stimulating research on how our
biological inheritance at least partially influences our traits and behaviors.

Lifespan Development and Evolutionary Psychology

As we consider development from conception through the lifespan, there will be many opportunities
to understand how evolutionary psychology enhances our understanding of development. For
instance, women and men do differ in their preferences for a few key qualities in long-term mating,
because of somewhat distinct adaptive concerns. Modern women have inherited the evolutionary
trait to desire mates who possess resources, have qualities linked with acquiring resources (e.g.,
ambition, wealth, industriousness), and are willing to share those resources with them. On the other
hand, men more strongly desire youth and health in women, as both are cues to fertility. These male
and female differences have historically been universal in humans.

Just because a psychological adaptation was advantageous in our history, does not mean it’s still
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useful today. For example, even though women may have preferred men with resources in previous
generations, our modern society has advanced such that these preferences are no longer necessary.
Nonetheless, it’s important to consider how our evolutionary history has shaped our automatic or
“instinctual” desires and reflexes of today so that we can better shape them for the future ahead.

As we follow the journey of life, from conception to death, think about how the theory of natural
selection and the concepts of evolutionary psychology can enlighten our understanding of why
some automatic reflexes or instinctual desires are more common than others. Remember that the
end product of the theory of evolution by natural selection is successful survival and reproduction.
Can you think of some ways that the ultimate goal of reproductive success affects our selection of a
mate, how we parent young children, why we are motivated to achieve certain goals, or what
differentiates families with traditionally longer lifespans? In order to achieve reproductive success,
the theory of evolution by natural selection states that organisms should be suited to their
environment. Think about how different environments or cultures require different traits for
successful survival and reproduction. Can you think of some ways that we may be changing to be
better suited to our changing culture?

Link to Learning

David Buss is one of the leading researchers in evolutionary psychology. In David Buss’s
Ted Talk, he explains several theories related to the selection of sexual partners, mating
preferences, and infidelity.

Heredity and Chromosomes

Gametes

There are two types of sex cells or gametes involved in reproduction: the male gametes, or sperm,
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and female gametes, or ova. The male gametes are produced in

the testes through a process called spermatogenesis, which
begins at about 12 years of age. The female gametes, which are
stored in the ovaries, are present at birth but are immature. Each
ovary contains about 250,000 ova but only about 400 of these
will become mature eggs (Mackon & Fauser, 2000; Rome,
1998). Beginning at puberty, one ovum ripens and is released
about every 28 days, a process called oogenesis.

After the ovum or egg ripens and is released from the ovary, it is Figure 2. The Female Reproductive
System.
drawn into the fallopian tube and in 3 to 4 days, reaches the
uterus. It is typically fertilized in the fallopian tube and continues its journey to the uterus. At
ejaculation, millions of sperm are released into the vagina, but only a few reach the egg and
typically, only one fertilizes the egg. Once a single sperm has entered the wall of the egg, the wall
becomes hard and prevents other sperm from entering. After the sperm has entered the egg, the tail
of the sperm breaks off and the head of the sperm, containing the genetic information from the
father, unites with the nucleus of the egg. As a result, a new cell is formed. This cell, containing the
combined genetic information from both parents, is referred to as a zygote.

Chromosomes

While other normal human cells have 46 chromosomes (or 23 pairs), gametes contain 23
chromosomes. Chromosomes are long threadlike structures found in a cell nucleus that contains
genetic material known as deoxyribonucleic acid (DNA). DNA is a helix-shaped molecule made
up of nucleotide base pairs [adenine (A), guanine (G), cytosine (C), and thymine (T)]. In each
chromosome, sequences of DNA make up genes that control or partially control a number of visible
characteristics, known as traits, such as eye color, hair color, and so on. A single gene may have
multiple possible variations or alleles. An allele is a specific version of a gene. So, a given gene
may code for the trait of hair color, and the different alleles of that gene affect which hair color an
individual has.

In a process called meiosis, segments of the chromosomes from each parent form pairs, and genetic
segments are exchanged as determined by chance. Because of the unpredictability of this exchange,
the likelihood of having offspring that are genetically identical (and not twins) is one in trillions
(Gould & Keeton, 1997). Genetic variation is important because it allows a species to adapt so that
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those who are better suited to the

environment will survive and reproduce,
which is an important factor in natural
selection.

Genotypes and Phenotypes

When a sperm and egg fuse, their 23

chromosomes pair up and create a zygote
with 23 pairs of chromosomes. Therefore,
each parent contributes half the genetic
information carried by the offspring; the
resulting physical characteristics of the
offspring (called the phenotype) are
Figure 3. Deoxyribonucleic acid (DNA) is a helix-shaped
molecule made up of nucleotide base pairs. Sequences of determined by the interaction of genetic
DNA make up genes. material supplied by the parents (called
the genotype). A person’s genotype is the
genetic makeup of that individual. Phenotype, on the other hand, refers to the individual’s inherited
physical characteristics.

Look in the mirror. What do you see, your genotype or your phenotype? What determines whether
or not genes are expressed? Actually, this is quite complicated. Some features follow the additive
pattern which means that many different genes contribute to a final outcome. Height and skin tone
are examples. In other cases, a gene might either be turned on or off depending on several factors,
including the gene with which it is paired or the inherited epigenetic tags.

Link To learning

Visit the webpage “What are DNA and Genes?” from the University of Utah to better
understand DNA and genes, then watch the video “What is Inheritance?” to learn how the
genes from parents pass on genetic information to their children.

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Determining the Sex of the Child

Twenty-two of those chromosomes from each parent are similar in length to a corresponding
chromosome from the other parent. However, the remaining chromosome looks like an X or a Y.
Half of the male’s sperm contains a Y chromosome and half contain an X. All of the ova contain X
chromosomes. If the child receives the combination of XY, the child will be genetically male. If it
receives the XX combination, the child will be genetically female.

Many potential parents have a clear preference for having a boy or a girl and would like to
determine the sex of the child. Through the years, a number of tips have been offered for potential
parents to maximize their chances of having either a son or daughter as they prefer. However, there
is not much scientific evidence to back these claims. Today, however, there is new technology
available called sperm sorting that makes it possible to isolate sperm containing either an X or a Y,
depending on the preference, and use that sperm to fertilize a mother’s egg. Preimplantation genetic
diagnosis (PGD) could also be used to select only embryos of the desired sex to be implanted during
in-vitro fertilization (IVF). However, these methods are controversial and both fertility centers and
medical organizations discourage it if there is no real medical reason to select gender.

Genetic Variation and Inheritance

Genetic variation, the genetic difference between individuals, is what contributes to a species’
adaptation to its environment. In humans, genetic variation begins with an egg, several million
sperm, and fertilization. The egg and the sperm each contain 23 chromosomes, which make up our
genes. A single gene may have multiple possible variations or alleles (a specific version of a gene),
resulting in a variety of combinations of inherited traits.

Genetic inheritance of traits for humans is based upon Gregor Mendel’s model of inheritance. For
genes on an autosome (any chromosome other than a sex chromosome), the alleles and their
associated traits are autosomal dominant or autosomal recessive. In this model, some genes are
considered dominant because they will be expressed. Others, termed recessive, are only expressed
in the absence of a dominant gene. Some characteristics which were once thought of as dominant-
recessive, such as eye color, are now believed to be a result of the interaction between several genes
(McKusick, 1998). Dominant traits include curly hair, facial dimples, normal vision, and dark
hair. Recessive characteristics include red hair, pattern baldness, and nearsightedness.

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Sickle cell anemia is an autosomal recessive disease; Huntington’s disease is an autosomal

dominant disease. Other traits are a result of partial dominance or co-dominance in which both
genes are influential. For example, if a person inherits both recessive genes for cystic fibrosis, the
disease will occur. But if a person has only one recessive gene for the disease, the person would be a
carrier of the disease.

In this example, we will call the normal gene “N,” and the gene for cystic fibrosis “c.” The normal
gene is dominant, which means that having the dominant allele either from one parent (Nc) or both
parents (NN) will always result in the phenotype associated with the dominant allele. When
someone has two copies of the same allele, they are said to be homozygous for that allele. When
someone has a combination of alleles for a given gene, they are said to be heterozygous. For
example, cystic fibrosis is a recessive disease which means that an individual will only have the
disease if they are homozygous for that recessive allele (cc).

Imagine that a woman who is a carrier of the cystic fibrosis gene has a child with a man who also is
a carrier of the same disease. What are the odds that their child would inherit the disease? Both the
woman and the man are heterozygous for this gene (Nc). We can expect the offspring to have a
25% chance of having cystic fibrosis (cc), a 50% chance of being a carrier of the disease (Nc), and a
25% chance of receiving two normal copies of the gene (NN).

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Figure 4. A Punnett square is a tool used to predict how

genes will interact in the production of offspring. The
capital N represents the dominant allele, and the lowercase
c represents the recessive allele. In the example of cystic
fibrosis, where N is the normal gene (dominant allele),
wherever a pair contains the dominant allele, N, you can
expect a phenotype that does not express the disease. You
can expect a cystic fibrosis phenotype only when there are
two copies of the c (recessive allele) which contains the gene
mutation that causes the disease.

Where do harmful genes that contribute to diseases like cystic fibrosis come from? Gene mutations
provide one source of harmful genes. A mutation is a sudden, permanent change in a gene. While
many mutations can be harmful or lethal, once in a while a mutation benefits an individual by
giving that person an advantage over those who do not have the mutation. Recall that the theory of
evolution asserts that individuals best adapted to their particular environments are more likely to
reproduce and pass on their genes to future generations. In order for this process to occur, there
must be competition—more technically, there must be variability in genes (and resultant traits) that
allow for variation in adaptability to the environment. If a population consisted of identical
individuals, then any dramatic changes in the environment would affect everyone in the same way,
and there would be no variation in selection. In contrast, diversity in genes and associated traits
allow some individuals to perform slightly better than others when faced with environmental
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change. This creates a distinct advantage for individuals best suited for their environments in terms
of successful reproduction and genetic transmission.

Link to Learning

Visit the Cystic Fibrosis Foundation to learn more about cystic fibrosis and learn how
a mutation in DNA leads to the disease.

Chromosomal Abnormalities and Genetic Testing

Chromosomal Abnormalities

A chromosomal abnormality occurs when a child

inherits too many or too few chromosomes. The
most common cause of chromosomal abnormalities
is the age of the mother. A 20-year-old woman has
a 1 in 800 chance of having a child with a common
chromosomal abnormality. A woman of 44,
however, has a one in 16 chance. It is believed that
the problem occurs when the ovum is ripening prior
to ovulation each month. As the mother ages, the
ovum is more likely to suffer abnormalities at this Figure 5. The three major single chromosome
time. mutations: deletion (1), duplication (2), and
inversion (3).

Another common cause of chromosomal

abnormalities occurs because the gametes do not divide evenly when they are forming. Therefore,
some cells have more than 46 chromosomes. In fact, it is believed that close to half of all zygotes
have an odd number of chromosomes. Most of these zygotes fail to develop and are spontaneously
aborted by the body. If the abnormal number occurs on pair # 21 or # 23, however, the individual
may have certain physical or other abnormalities.
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An altered chromosome structure may take several different forms, and result in various disorders or
malignancies:

Deletions: A portion of the chromosome is missing or deleted. Known disorders in humans

include Wolf-Hirschhorn syndrome, which is caused by partial deletion of the short arm of
chromosome 4; and Jacobsen syndrome also called the terminal 11q deletion disorder.
Duplications: A portion of the chromosome is duplicated, resulting in extra genetic material.
Known human disorders include Charcot-Marie-Tooth disease type 1A, which may be caused
by duplication of the gene encoding peripheral myelin protein 22 (PMP22) on chromosome 17.
Translocations: A portion of one chromosome is
transferred to another chromosome. There are
two main types of translocations:

Reciprocal translocation: Segments from

two different chromosomes have been
exchanged.
Robertsonian translocation: An entire
chromosome has attached to another at the
centromere – in humans, these only occur
with chromosomes 13, 14, 15, 21, and 22.
Inversions: A portion of the chromosome has
broken off, turned upside down, and reattached,
therefore the genetic material is inverted.
Insertions: A portion of one chromosome has
been deleted from its normal place and inserted
into another chromosome.
Rings: A portion of a chromosome has broken Figure 6. The two major two-chromosome
off and formed a circle or ring. This can happen mutations: insertion (1) and Translocation (2).
with or without loss of genetic material.
Isochromosome: Formed by the mirror image copy of a chromosome segment including the
centromere.

One of the most common chromosomal abnormalities is on pair # 21. Trisomy 21 occurs when there
are three rather than two chromosomes on #21. A person with Down syndrome has distinct facial
features, intellectual disability, and oftentimes heart and gastrointestinal disorders. Symptoms vary
from person to person and can range from mild to severe. With early intervention, the
life expectancy of persons with Down syndrome has increased in recent years. Keep in mind that
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there is as much variation in people with Down Syndrome as in most populations and those
differences need to be recognized and appreciated.

When the chromosomal abnormality is on pair #23, the result is a sex-linked chromosomal
abnormality. A person might have XXY, XYY, XXX, XO, or 45 or 47 chromosomes as a result. Two
of the more common sex-linked chromosomal disorders are Turner syndrome and Klinefelter
syndrome. Turner’s syndrome occurs in 1 of every 2,500 live female births when an ovum that
lacks a chromosome is fertilized by a sperm with an X chromosome (Carroll, 2007). The resulting
zygote has an XO composition. Fertilization by a Y sperm is not viable. Turner syndrome affects
cognitive functioning and sexual maturation. The external genitalia appear normal, but breasts and
ovaries do not develop fully and the woman does not menstruate. Turner’s syndrome also results in
short stature and other physical characteristics. Klinefelter syndrome (XXY) occurs in 1 out of 700
live male births and results when an ovum containing an extra X chromosome is fertilized by a Y
sperm. The Y chromosome stimulates the growth of male genitalia, but the additional X
chromosome inhibits this development. An individual with Klinefelter syndrome has some breast
development, infertility (this is the most common cause of infertility in males), and has low levels
of testosterone.

Prenatal Testing

Prenatal testing consists of prenatal screening and prenatal diagnosis, which are aspects of prenatal
care that focus on detecting problems with the pregnancy as early as possible. These may
be anatomic and physiologic problems with the health of the zygote, embryo, or fetus, either
before gestation even starts or as early in gestation as practical. Prenatal screening focuses on
finding problems among a large population with affordable and noninvasive methods. The most
common screening procedures are routine ultrasounds, blood tests, and blood pressure
measurement. Prenatal diagnosis focuses on pursuing additional detailed information once a
particular problem has been found, and can sometimes be more invasive.

Screening can detect problems such as neural tube defects, anatomical defects, chromosome
abnormalities, and gene mutations that would lead to genetic disorders and birth defects, such as
spina bifida, cleft palate, Downs Syndrome, Tay–Sachs disease, sickle cell anemia, thalassemia,
cystic fibrosis, muscular dystrophy, and fragile X syndrome. Some tests are designed to discover
problems that primarily affect the health of the mother, such as PAPP-A to detect pre-eclampsia or

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glucose tolerance tests to diagnose gestational diabetes. Screening can also detect anatomical
defects such as hydrocephalus, anencephaly, heart defects, and amniotic band syndrome.

Common prenatal diagnosis procedures include amniocentesis and chorionic villus sampling.
Because of the miscarriage and fetal damage risks associated with amniocentesis and CVS
procedures, many women prefer to first undergo screening so they can find out if the fetus’ risk of
birth defects is high enough to justify the risks of invasive testing. Screening tests yield a risk score
which represents the chance that the baby has the birth defect; the most common threshold for high-
risk is 1:270. A risk score of 1:300 would, therefore, be considered low-risk by many physicians.
However, the trade-off between the risk of birth defects and risk of complications from invasive
testing is relative and subjective; some parents may decide that even a 1:1000 risk of birth defects
warrant an invasive test while others wouldn’t opt for an invasive test even if they had a 1:10 risk
score.

There are three main purposes of prenatal diagnosis: (1) to enable timely medical or surgical
treatment of a condition before or after birth, (2) to give the parents the chance to abort a fetus with
the diagnosed condition, and (3) to give parents the chance to prepare psychologically, socially,
financially, and medically for a baby with a health problem or disability, or for the likelihood of
stillbirth. Having this information in advance of birth means that healthcare staff, as well as parents,
can better prepare themselves for the delivery of a child with a health problem. For example, Down
Syndrome is associated with cardiac defects that may need intervention immediately upon birth.

The American College of Obstetricians and Gynecologists (ACOG) guidelines currently

recommend that all pregnant women, regardless of age, be offered invasive testing to obtain a
definitive diagnosis of certain birth defects. Therefore, most physicians offer diagnostic testing to all
their patients, with or without prior screening, and let the patient decide.

Behavioral Genetics

Behavioral geneticists study how individual differences arise, in the present, through the interaction
of genes and the environment. When studying human behavior, behavioral geneticists often employ
twin and adoption studies to research questions of interest. Twin studies compare the rates that a
given behavioral trait is shared among identical and fraternal twins; adoption studies compare those
rates among biologically related relatives and adopted relatives. Both approaches provide some
insight into the relative importance of genes and environment for the expression of a given trait.

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The evolutionary perspective encompasses one of the fastest-growing areas within the field of
lifespan development: behavioral genetics. Behavioral genetics is a field of scientific research that
uses genetic methods to investigate the nature and origins of individual differences in behavior and
studies the effects of heredity on behavior. Behavioral geneticists strive to understand how we might
inherit certain behavioral traits and how the environment influences whether we actually displayed
those traits. It also considers how genetic factors may influence psychological disorders such as
schizophrenia, depression, and substance abuse.

Nature or Nurture?

For decades, scholars have carried on the “nature/nurture” debate. For any particular feature, those
on the “nature” side would argue that heredity plays the most important role in bringing about that
feature. Those on the “nurture” side would argue that one’s environment is most significant in
shaping the way we are. This debate continues in questions about what makes us masculine or
feminine (Lippa, 2002), concerns about vision (Mutti, Kadnik, & Adams, 1996), and many other
developmental issues.

Most scholars agree that there is a constant interplay between the two forces. It is difficult to isolate
the root of any single behavior as a result solely of nature or nurture, and most scholars believe that
even determining the extent to which nature or nurture impacts a human feature is difficult to
answer. In fact, almost all human features are polygenic (a result of many genes)
and multifactorial (a result of many factors, both genetic and environmental). It is as if one’s genetic
make-up sets up a range of possibilities, which may or may not be realized depending upon one’s
environmental experiences. For instance, a person might be genetically predisposed to develop
diabetes, but the person’s lifestyle may help bring about the disease.

When you think about your own family history, it is easy to see that there are certain personality
traits, behavioral characteristics, and medical conditions that are more common than others. This is
the reason that doctors ask you about your family medical history. While genetic predisposition is
important to consider, there are some family members who, for a variety of reasons, seemed to defy
the odds of developing these conditions. These differences can be explained in part by the effect
of epigenetic (above the genome) changes.

The Epigenetic Framework

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The term “epigenetic” has been used in developmental psychology to describe psychological
development as the result of an ongoing, bi-directional interchange between heredity and the
environment. Gottlieb (1998; 2000; 2002) suggests an analytic framework for the nature/nurture
debate that recognizes the interplay between the environment, behavior, and genetic expression.
This bidirectional interplay suggests that the environment can affect the expression of genes just as
genetic predispositions can impact a person’s potentials. Likewise, environmental circumstances can
trigger symptoms of a genetic disorder. For example, a person predisposed genetically for type 2
diabetes may trigger the disease through poor diet and little exercise.

The developmental psychologist Erik Erikson wrote of an epigenetic principle in his book Identity:
Youth and Crisis (1968), encompassing the notion that we develop through an unfolding of our
personality in predetermined stages, and that our environment and surrounding culture influence
how we progress through these stages. This biological unfolding in relation to our socio-cultural
settings is done in stages of psychosocial development, where “progress through each stage is in
part determined by our success, or lack of success, in all the previous stages.”

In typical human families, children’s biological parents raise them, so it is very difficult to know
whether children act like their parents due to genetic (nature) or environmental (nurture) reasons.
Nevertheless, despite our restrictions on setting up human-based experiments, we do see real-world
examples of nature-nurture at work in the human sphere—though they only provide partial answers
to our many questions. The science of how genes and environments work together to influence
behavior is called behavioral genetics. The easiest opportunity we have to observe this is
the adoption study. When children are put up for adoption, the parents who give birth to them are
no longer the parents who raise them. Children aren’t assigned to random adoptive parents in order
to suit the particular interests of a scientist but adoption still tells us some interesting things, or at
least confirms some basic expectations. For instance, if the biological child of tall parents were
adopted into a family of short people, do you suppose the child’s growth would be affected? What
about the biological child of a Spanish-speaking family adopted at birth into an English-speaking
family? What language would you expect the child to speak? And what might these outcomes tell
you about the difference between height and language in terms of nature-nurture?

Monozygotic and Dizygotic Twins

Another option for observing nature-nurture in humans involves twin studies. To analyze nature-
nurture using twins, we compare the similarity of monozygotic and dizygotic
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pairs. Monozygotic twins occur when a single zygote or fertilized egg splits apart in the first two
weeks of development. The result is the creation of two separate but genetically identical offspring.
About one-third of twins are monozygotic twins. Monozygotic twins occur in birthing at a rate of
about 3 in every 1000 deliveries worldwide (about 0.3% of the world population). Monozygotic
twins are genetically nearly identical and they are always the same sex unless there has been a
mutation during development. The children of monozygotic twins test genetically as half-siblings
(or full siblings, if a pair of monozygotic twins reproduces with another pair of identical twins or
with the same person), rather than first cousins.

Sometimes two eggs or ova are released and fertilized by two separate sperm. The result
is dizygotic or fraternal twins. About two-thirds of twins are dizygotic. These two individuals share
the same amount of genetic material as would any two children from the same mother and father.
Older mothers are more likely to have dizygotic twins than are younger mothers and couples who
use fertility drugs are also more likely to give birth to dizygotic twins. Consequently, there has been
an increase in the number of fraternal twins in recent years (Bortolus et al., 1999). In vitro
fertilization (IVF) techniques are more likely to create dizygotic twins. For IVF deliveries, there are
nearly 21 pairs of twins for every 1,000.

In the uterus, a majority of monozygotic twins (60–70%) share the same placenta but have
separate amniotic sacs. The placenta is a temporary organ that connects the developing fetus via
the umbilical cord to the uterine wall to allow nutrient uptake, thermo-regulation, waste elimination,
and gas exchange via the mother’s blood supply. The amniotic sac (also called the bag of waters
or the membranes), is a thin but tough transparent pair of membranes that hold a
developing embryo (and later fetus) until shortly before birth. In 18–30% of monozygotic twins
each fetus has a separate placenta and a separate amniotic sac. A small number (1–2%) of
monozygotic twins share the same placenta and amniotic sac. Fraternal twins each have their own
placenta and own amniotic sac.

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Figure 7. Monozygotic twins come from a

single zygote and generally share the same
placenta, although some (18-30%) have
separate placentas. Dizygotic twins come from
two separately fertilized eggs and have their
own placentas and amniotic sacs.

Monozygotic (one egg/identical) twins can be categorized into four types depending on the timing
of the separation and duplication of cells. Various types of chorionicity and amniosity (how the
baby’s sac looks) in monozygotic twins are a result of when the fertilized egg divides. This is
known as placentation.

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Figure 8. Various types of chorionicity and amniosity

(how the baby’s sac looks) in monozygotic (one
egg/identical) twins as a result of when the fertilized
egg divides (Author Kevin Dufenbach)

Conjoined twins

Conjoined twins are monozygotic twins whose bodies are joined together during pregnancy. This
occurs when the zygote starts to split after day 12 following fertilization and fails to separate
completely. This condition occurs in about 1 in 50,000 human pregnancies. Most conjoined twins
are now evaluated for surgery to attempt to separate them into separate functional bodies. The
degree of difficulty rises if a vital organ or structure is shared between twins, such as
the brain, heart, or liver.

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Vanishing twins

Researchers suspect that as many as 1 in 8 pregnancies start out as multiples, but only a single fetus
is brought to full term because the other fetus has died very early in the pregnancy and has not been
detected or recorded. Early obstetric ultrasonography exams sometimes reveal an “extra” fetus,
which fails to develop and instead disintegrates and vanishes in the uterus. There are several reasons
for the “vanishing” fetus, including it being embodied or absorbed by the other fetus, placenta or the
mother. This is known as vanishing twin syndrome. Also, in an unknown proportion of cases, two
zygotes may fuse soon after fertilization, resulting in a single chimeric embryo, and, later, fetus.

Twin Studies

Using the features of height and spoken language as examples, let’s take a look at how nature and
nurture apply: identical twins, unsurprisingly, are almost perfectly similar for height. The heights of
fraternal twins, however, are like any other sibling pairs: more similar to each other than to people
from other families, but hardly identical. This contrast between twin types gives us a clue about the
role genetics plays in determining height.

Now consider
spoken language.
If one identical
twin speaks
Spanish at home,
the co-twin with
whom she is raised
almost certainly
does too. But the
same would be
true for a pair of
fraternal twins
raised together. In Figure 9. Identical twins Laurent and Larry Nicolas Bourgeois, also known as the Les
Twins, are internationally renowned dancers.
terms of spoken
language, fraternal
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twins are just as similar as identical twins, so it appears that the genetic match of identical twins
doesn’t make much difference.

Twin and adoption studies are two instances of a much broader class of methods for observing
nature-nurture called quantitative genetics, the scientific discipline in which similarities among
individuals are analyzed based on how biologically related they are. We can do these studies with
siblings and half-siblings, cousins, and twins who have been separated at birth and raised separately
(Bouchard, Lykken, McGue, & Segal, 1990). Such twins are very rare and play a smaller role than
is commonly believed in the science of nature-nurture, or with entire extended families (Plomin,
DeFries, Knopik, & Neiderhiser, 2012).

It would be satisfying to be able to say that nature-nurture studies have given us conclusive and
complete evidence about where traits come from, with some traits clearly resulting from genetics
and others almost entirely from environmental factors, such as child-rearing practices and personal
will; but that is not the case. Instead, everything has turned out to have some footing in genetics.
The more genetically-related people are, the more similar they are—for everything: height, weight,
intelligence, personality, mental illness, etc. Sure, it seems like common sense that some traits have
a genetic bias. For example, adopted children resemble their biological parents even if they have
never met them, and identical twins are more similar to each other than are fraternal twins. And
while certain psychological traits, such as personality or mental illness (e.g., schizophrenia), seem
reasonably influenced by genetics, it turns out that the same is true for political attitudes, how much
television people watch (Plomin, Corley, DeFries, & Fulker, 1990), and whether or not they get
divorced (McGue & Lykken, 1992).

What you’ll learn to do: explain the main stages of prenatal

development

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How did you come to be who you are? From beginning as a one-cell structure to your birth,
your prenatal development occurred in an orderly and delicate sequence. There are three stages of
prenatal development: germinal, embryonic, and fetal. Keep in mind that this is different than the
three trimesters of pregnancy. Let’s take a look at what happens to the developing baby in each of
these stages.

Learning outcomes

Differentiate between development during the germinal, embryonic, and fetal

periods
Examine risks to prenatal development posed by exposure to teratogens
Explain potential complications of pregnancy and delivery

Prenatal Development

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“The body of the unborn baby is more complex than ours. The preborn baby has several
extra parts to his body which he needs only so long as he lives inside his mother. He has his
own space capsule, the amniotic sac. He has his own lifeline, the umbilical cord, and he has
his own root system, the placenta. These all belong to the baby himself, not to his mother.
They are all developed from his original cell.”

WATCH IT: TED-ED: The Surprising Effects of Pregnancy on the Mother: Muscles
and joints shift and jostle. The heart’s pounding rhythm speeds up. Blood roars through
arteries and veins. Over the course of a pregnancy, every organ in the body changes.
Initiated by a range of hormones, these changes begin as soon as pregnancy begins.
Explore what we know— and don’t know— about pregnancy’s effects on the body and
brain.

Periods of Prenatal Development

Let’s take a look at some of the changes that take place during each of the three periods of prenatal
development: the germinal period, the embryonic period, and the fetal period.

The Germinal Period (Weeks 1-2)

Conception occurs when a sperm fertilizes an egg and forms a zygote, which begins as a one-cell
structure. The mother and father’s DNA is passed on to the child at the moment of conception. The
genetic makeup and sex of the baby are set at this point. The germinal period (about 14 days in
length) lasts from conception to implantation of the zygote (fertilized egg) in the lining of the
uterus.

During the first week after conception, the zygote divides and multiplies, going from a one-cell
structure to two cells, then four cells, then eight cells, and so on. The process of cell division is

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called mitosis. After the fourth division, differentiation

of the cells begins to occur as well. Differentiated cells
become more specialized, forming different organs and
body parts. After 5 days of mitosis, there are 100 cells,
and after 9 months there are billions of cells. Mitosis is
a fragile process, and fewer than one-half of all zygotes
survive beyond the first two weeks (Hall, 2004).

Figure 1. Sperm and Ovum at Conception After the zygote divides for about 7–10 days and has
150 cells, it travels down the fallopian tubes and
implants itself in the lining of the uterus. It’s estimated that about 60 percent of natural conceptions
fail to implant in the uterus. The rate is higher for in vitro conceptions. Once the zygote attaches to
the uterus, the next stage begins.

The Embryonic Period (Weeks 3-8)

The embryonic period begins once the zygote is implanted in the

uterine wall. It lasts from the third through the eighth week after
conception. Upon implantation, this multi-cellular organism is called
an embryo. Now blood vessels grow, forming the placenta.
The placenta is a structure connected to the uterus that provides
nourishment and oxygen from the mother to the developing embryo
via the umbilical cord.

During this period, cells continue to differentiate. Basic structures of

the embryo start to develop into areas that will become the head,
chest, and abdomen. During the embryonic stage, the heart begins to
beat and organs form and begin to function. At 22 days after
Figure 2. Human Embryo
conception, the neural tube forms along the back of the embryo,
developing into the spinal cord and brain.

Growth during prenatal development occurs in two major directions: from head to tail
(cephalocaudal development) and from the midline outward (proximodistal development). This
means that those structures nearest the head develop before those nearest the feet and those

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structures nearest the torso develop before those away from the center of the body (such as hands
and fingers).

The head develops in the fourth week and the precursor to the heart begins to pulse. In the early
stages of the embryonic period, gills and a tail are apparent. But by the end of this stage, they
disappear and the organism takes on a more human appearance. The embryo is approximately 1
inch in length and weighs about 4 grams at the end of this period. The embryo can move and
respond to touch at this time.

About 20 percent of organisms fail during the embryonic period, usually due to gross chromosomal
abnormalities. As in the case of the germinal period, often the mother does not yet know that she is
pregnant. It is during this stage that the major structures of the body are taking form making the
embryonic period the time when the organism is most vulnerable to the greatest amount of damage
if exposed to harmful substances. Potential mothers are not often aware of the risks they introduce
to the developing child during this time.

The Fetal Period (Weeks 9-40)

When the organism is about nine weeks old, the embryo

is called a fetus. At this stage, the fetus is about the size
of a kidney bean and begins to take on the recognizable
form of a human being as the “tail” begins to disappear.

From 9–12 weeks, the sex organs begin to differentiate.

By the 12th week, the fetus has all its body parts
including external genitalia. In the following weeks, the
fetus will develop hair, nails, teeth and the excretory
Figure 3. A fetus at 10 weeks of development. and digestive systems will continue to develop. At the
end of the 12th week, the fetus is about 3 inches long
and weighs about 28 grams.

At about 16 weeks, the fetus is approximately 4.5 inches long. Fingers and toes are fully developed,
and fingerprints are visible. During the 4-6th months, the eyes become more sensitive to light and
hearing develops. The respiratory system continues to develop. Reflexes such as sucking,
swallowing, and hiccuping develop during the 5th month. Cycles of sleep and wakefulness are
present at that time as well. Throughout the fetal stage, the brain continues to grow and develop,
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nearly doubling in size from weeks 16 to 28. The majority of the neurons in the brain have
developed by 24 weeks although they are still rudimentary and the glial or nurse cells that support
neurons continue to grow. At 24 weeks the fetus can feel pain (Royal College of Obstetricians and
Gynecologists, 1997).

The first chance of survival outside the womb, known as the age of viability is reached at about 22
to 26 weeks (Moore & Persaud, 1998). By the time the fetus reaches the sixth month of
development (24 weeks), it weighs up to 1.4 pounds. The hearing has developed, so the fetus can
respond to sounds. The internal organs, such as the lungs, heart, stomach, and intestines, have
formed enough that a fetus born prematurely at this point has a chance to survive outside of the
mother’s womb.

Between the 7th and 9th months, the fetus is primarily preparing for birth. It is exercising its
muscles, its lungs begin to expand and contract. It is developing fat layers under the skin. The fetus
gains about 5 pounds and 7 inches during this last trimester of pregnancy which includes a layer of
fat gained during the 8th month. This layer of fat serves as insulation and helps the baby regulate
body temperature after birth.

Around 36 weeks, the fetus is almost ready for birth. It weighs about 6 pounds and is about 18.5
inches long, and by week 37 all of the fetus’s organ systems are developed enough that it could
survive outside the mother’s uterus without many of the risks associated with premature birth. The
fetus continues to gain weight and grow in length until approximately 40 weeks. By then, the fetus
has very little room to move around and birth becomes imminent.

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Figure 4. During the fetal stage, the baby’s brain develops and the body adds size and weight until the fetus
reaches full-term development.

Environmental Risks

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Teratology

Good prenatal care is essential. The developing child is most at risk for some of the most severe
problems during the first three months of development. Unfortunately, this is a time at which most
mothers are unaware that they are pregnant. It is estimated that 10% of all birth defects are caused
by prenatal exposure or teratogen. Teratogens are factors that can contribute to birth defects which
include some maternal diseases, drugs, alcohol, and stress. These exposures can also include
environmental and occupational exposures. Today, we know many of the factors that can jeopardize
the health of the developing child. Teratogen-caused birth defects are potentially preventable.

The study of factors that contribute to birth defects is called teratology. Teratogens are usually
discovered after an increased prevalence of a particular birth defect. For example, in the early
1960s, a drug known as thalidomide was used to treat morning sickness. Exposure of the fetus
during this early stage of development resulted in cases of phocomelia, a congenital malformation
in which the hands and feet are attached to abbreviated arms and legs.

A Look at Some Teratogens

Alcohol

One of the most commonly used teratogens is alcohol. Because half of all pregnancies in the United
States are unplanned, it is recommended that women of child-bearing age take great caution against
drinking alcohol when not using birth control and when pregnant (Surgeon General’s Advisory on
Alcohol Use During Pregnancy, 2005). Alcohol consumption, particularly during the second month
of prenatal development, but at any point during pregnancy, may lead to neurocognitive and
behavioral difficulties that can last a lifetime.

There is no acceptable safe limit for alcohol use during pregnancy, but binge drinking (5 or more
drinks on a single occasion) or having 7 or more drinks during a single week places a child at
particularly high risk. In extreme cases, alcohol consumption can lead to fetal death, but more
frequently it can result in fetal alcohol spectrum disorders (FASD). This terminology is now used
when looking at the effects of exposure and replaces the term fetal alcohol syndrome. It is preferred
because it recognizes that symptoms occur on a spectrum and that all individuals do not have the
same characteristics. Children with FASD share certain physical features such as flattened noses,
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small eye openings, small heads, intellectual developmental

delays, and behavioral problems. Those with FASD are more
at risk for lifelong problems such as criminal behavior,
psychiatric problems, and unemployment (CDC, 2006).

The terms alcohol-related neurological disorder (ARND) and

alcohol-related birth defects (ARBD) have replaced the term
Fetal Alcohol Effects to refer to those with less extreme
symptoms of FASD. ARBD includes kidney, bone, and heart
problems.

Tobacco Figure 5. Some distinguishing

characteristics of fetal alcohol spectrum
disorders include more narrow eye
Smoking is also considered a teratogen because nicotine openings, A smooth philtrum, meaning a
smooth area between the upper lip and
travels through the placenta to the fetus. When the mother the nose, and a thin upper lip.
smokes, the developing baby experiences a reduction in
blood oxygen levels. Tobacco use during pregnancy has been associated with low birth weight,
placenta previa, birth defects, preterm delivery, fetal growth restriction, and sudden infant death
syndrome. Smoking in the month before getting pregnant and throughout pregnancy increases the
chances of these risks. Quitting smoking before getting pregnant is best. However, for women who
are already pregnant, quitting as early as possible can still help protect against some health problems
for the mother and baby.

Drugs

Prescription, over-the-counter, or recreational drugs can have serious teratogenic effects. In general,
if medication is required, the lowest dose possible should be used. Combination drug therapies and
first trimester exposures should be avoided. Almost three percent of pregnant women use illicit
drugs such as marijuana, cocaine, Ecstasy, and other amphetamines, and heroin. These drugs can
cause low birth-weight, withdrawal symptoms, birth defects, or learning or behavioral problems.
Babies born with a heroin addiction need heroin just like an adult addict. The child will need to be
gradually weaned from the heroin under medical supervision; otherwise, the child could have
seizures and die.

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Environmental Chemicals

Environmental chemicals can include exposure to a wide array of agents including pollution,
organic mercury compounds, herbicides, and industrial solvents. Some environmental pollutants of
major concern include lead poisoning, which is connected with low birth weight and slowed
neurological development. Children who live in older housing in which lead-based paints have been
used have been known to eat peeling paint chips thus being exposed to lead. The chemicals in
certain herbicides are also potentially damaging. Radiation is another environmental hazard that a
pregnant woman must be aware of. If a mother is exposed to radiation, particularly during the first
three months of pregnancy, the child may suffer some congenital deformities. There is also an
increased risk of miscarriage and stillbirth. Mercury leads to physical deformities and intellectual
disabilities (Dietrich, 1999).

Sexually Transmitted Infections

Sexually transmitted infections (STIs) can complicate pregnancy and may have serious effects on
both the mother and the developing baby. Most prenatal care today includes testing for STIs, and
early detection is important. STIs, such as chlamydia, gonorrhea, syphilis, trichomoniasis, and
bacterial vaginosis can all be treated and cured with antibiotics that are safe to take during
pregnancy. STIs that are caused by viruses, like genital herpes, hepatitis B, or HIV cannot be cured.
However, in some cases these infections can be treated with antiviral medications or other
preventive measures can be taken to reduce the risk of passing the infection to the baby.

Maternal Diseases

Maternal illnesses increase the chance that a baby will be born with a birth defect or have a chronic
health problem. Some of the diseases that are known to potentially have an adverse effect on the
fetus include diabetes, cytomegalovirus, toxoplasmosis, Rubella, varicella, hypothyroidism, and
Strep B. If the mother contracts Rubella during the first three months of pregnancy, damage can
occur in the eyes, ears, heart, or brain of the unborn child. On a positive note, Rubella has been
nearly eliminated in the industrial world due to the vaccine created in 1969. Diagnosing these
diseases early and receiving appropriate medical care can help improve the outcomes. Routine
prenatal care now includes screening for gestational diabetes and Strep B.

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Maternal Stress

Stress represents the effects of any factor able to threaten the homeostasis of an organism; these
either real or perceived threats are referred to as the “stressors” and comprise a long list of potential
adverse factors, which can be emotional or physical. Because of a link in blood supply between a
mother and fetus, it has been found that stress can leave lasting effects on a developing fetus, even
before a child is born. The best-studied outcomes of fetal exposure to maternal prenatal stress are
preterm birth and low birth weight. Maternal prenatal stress is also considered responsible for a
variety of changes of the child’s brain, and a risk factor for conditions such as behavioral problems,
learning disorders, high levels of anxiety, attention deficit hyperactivity disorder, autism, and
schizophrenia. Furthermore, maternal prenatal stress has been associated with a higher risk for a
variety of immune and metabolic changes in the child such as asthma, allergic disorders,
cardiovascular diseases, hypertension, hyperlipidemia, diabetes, and obesity (Konstantinos et al.,
2017).

WHAT DO YOU THINK? Should Women Who Use Drugs

During Pregnancy Be Arrested and Jailed?

As you now know, women who use drugs or alcohol during pregnancy can cause
serious lifelong harm to their child. Some people have advocated mandatory screenings
for women who are pregnant and have a history of drug abuse, and if the women
continue using, to arrest, prosecute, and incarcerate them (Figdor & Kaeser, 1998).
This policy was tried in Charleston, South Carolina, as recently as 20 years ago. The
policy was called the Interagency Policy on Management of Substance Abuse During
Pregnancy and had disastrous results.

The Interagency Policy applied to patients attending the obstetrics clinic at

MUSC, which primarily serves patients who are indigent or on Medicaid. It
did not apply to private obstetrical patients. The policy required patient
education about the harmful effects of substance abuse during pregnancy. . . .
[A] statement also warned patients that protection of unborn and newborn
children from the harms of illegal drug abuse could involve the Charleston
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police, the Solicitor of the Ninth Judicial Court, and the Protective Services
Division of the Department of Social Services (DSS). (Jos, Marshall, &
Perlmutter, 1995, pp. 120–121)

This policy seemed to deter women from seeking prenatal care, deterred them from
seeking other social services, and was applied solely to low-income women, resulting
in lawsuits. The program was canceled after 5 years, during which 42 women were
arrested. A federal agency later determined that the program involved human
experimentation without the approval and oversight of an institutional review board
(IRB). What were the flaws in the program and how would you correct them? What are
the ethical implications of charging pregnant women with child abuse?

Factors influencing prenatal risks

There are several considerations in determining the type and amount of damage that might result
from exposure to a particular teratogen (Berger, 2004). These include:

The timing of the exposure: Structures in the body are vulnerable to the most severe damage
when they are forming. If a substance is introduced during a particular structure’s critical
period (time of development), the damage to that structure may be greater. For example, the
ears and arms reach their critical periods at about 6 weeks after conception. If a mother
exposes the embryo to certain substances during this period, the arms and ears may be
malformed.
The amount of exposure: Some substances are not harmful unless the amounts reach a certain
level. The critical level depends in part on the size and metabolism of the mother.
Genetics: Genetic make-up also plays a role in the impact a particular teratogen might have on
the child. This is suggested by fraternal twin studies who are exposed to the same prenatal
environment, yet do not experience the same teratogenic effects. The genetic make-up of the
mother can also have an effect; some mothers may be more resistant to teratogenic effects than
others.
Being male or female: Males are more likely to experience damage due to teratogens than are
females. It is believed that the Y chromosome, which contains fewer genes than the X, may
have an impact.
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Figure 6. Critical Periods of Prenatal Development. This image summarizes the three
developmental periods in prenatal development. The blue images indicate where major
development is happening and the aqua indicate where refinement is happening. As shown, the
majority of organs are particularly susceptible during the embryonic period. The central nervous
system still continues to develop in major ways through the fetal period as well.

Complications of Pregnancy and Delivery

There are a number of common side effects of pregnancy. Not everyone experiences all of these nor
do women experience them to the same degree. And although they are considered “minor” these
problems are potentially very uncomfortable. These side effects include nausea (particularly during
the first 3-4 months of pregnancy as a result of higher levels of estrogen in the system), heartburn,
gas, hemorrhoids, backache, leg cramps, insomnia, constipation, shortness of breath or varicose
veins (as a result of carrying a heavy load on the abdomen). What is the cure? Delivery!

Major Complications

The following are some serious complications of pregnancy that can pose health risks to mother and
child and that often require special care.
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Gestational diabetes is when a woman

without diabetes develops high blood sugar levels
during pregnancy.
Hyperemesis gravidarum is the presence of severe and
persistent vomiting, causing dehydration and weight
loss. It is more severe than the more common morning
sickness.
Preeclampsia is gestational hypertension. Severe
preeclampsia involves blood pressure over 160/110 with
additional signs. Eclampsia is seizures in a pre-eclamptic
patient.
Deep vein thrombosis is the formation of a blood clot in
a deep vein, most commonly in the legs.
A pregnant woman is more susceptible to infections.
This increased risk is caused by an increased immune
tolerance in pregnancy to prevent an immune reaction Figure 7. Pregnancy affects women in
different ways; some notice few adverse
against the fetus.
side effects, while others feel high levels
Peripartum cardiomyopathy is a decrease in heart of discomfort, or develop more serious
function which occurs in the last month of pregnancy, or complications.

up to six months post-pregnancy.

Maternal Mortality

Maternal mortality is unacceptably high. About 295,000 women died during and following
pregnancy and childbirth in 2017. The vast majority of these deaths (94%) occurred in low-resource
settings, and most could have been prevented. The high number of maternal deaths in some areas of
the world reflects inequalities in access to quality health services and highlights the gap between
rich and poor. The MMR in low-income countries in 2017 is 462 per 100,000 live births versus 11
per 100,000 live births in high-income countries. The high number of maternal deaths in some areas
of the world reflects inequities in access to health services and highlights the gap between rich and
poor.

Women in less developed countries have, on average, many more pregnancies than women in
developed countries, and their lifetime risk of death due to pregnancy is higher. A woman’s lifetime
risk of maternal death is the probability that a 15-year-old woman will eventually die from a

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maternal cause. In high-income countries, this is 1 in 5400, versus 1 in 45 in low-income countries.

Every day in 2017, approximately 810 women died from preventable causes related to pregnancy
and childbirth.

Figure 8. The number of women and girls who died each year from complications of pregnancy and
childbirth declined from 451,000 in 2000 to 295,000 in 2017. These improvements are particularly
remarkable in light of rapid population growth in many of the countries where maternal deaths are
highest. Still, over 800 women are dying each day from complications in pregnancy and
childbirth. And for every woman who dies, approximately 20 others suffer serious injuries,
infections or disabilities. Source: UNICEF, [Link]
mortality/.Even though maternal mortality in the United States is relatively rare today because of
advances in medical care, it is still an issue that needs to be addressed. Sadly, about 700 women die
each year in the United States as a result of pregnancy or delivery complications. The Centers for
Disease Control and Prevention define a pregnancy-related death as the death of a woman while
pregnant or within 1 year of the end of a pregnancy–regardless of the outcome, duration, or site of
the pregnancy–from any cause related to or aggravated by the pregnancy or its management, but not
from accidental or incidental causes.
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Since the Pregnancy Mortality Surveillance System was implemented, the number of reported
pregnancy-related deaths in the United States steadily increased from 7.2 deaths per 100,000 live
births in 1987 to 17.3 deaths per 100,000 live births in 2017. The graph above shows trends in
pregnancy-related mortality ratios between 1987 and 2017 (the latest available year of data).

The reasons for the overall increase in pregnancy-related mortality are unclear. What do you think
are some reasons for this surprising increase in the United States? What can be done to change this
statistic?

Watch It: Maternal Mortality in the United States

In the United States, black women are disproportionately more likely to die from
complications related to pregnancy or childbirth than any other race; they are three or four
times more likely than white women to die due to pregnancy-related death and are more
likely to receive worse maternal care. Black women from higher income groups and with
advanced education levels also have heightened risks—even tennis superstar Serena

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Williams had near-deadly complications during the birth of her daughter, Olympia. Why is
this the case in our modern world? Watch this video to learn more.

Considerable racial/ethnic disparities in pregnancy-related mortality exist.2,3 During 2014–

2017, the pregnancy-related mortality ratios were:

41.7 deaths per 100,000 live births for non-Hispanic Black women.
28.3 deaths per 100,000 live births for non-Hispanic American Indian or Alaska
Native women.
13.8 deaths per 100,000 live births for non-Hispanic Asian or Pacific Islander
women.
13.4 deaths per 100,000 live births for non-Hispanic White women.
11.6 deaths per 100,000 live births for Hispanic or Latina women.

Variability in the risk of death by race/ethnicity may be due to several factors including
access to care, quality of care, prevalence of chronic diseases, structural racism, and
implicit biases.

Why do women die in Pregnancy and Childbirth Worldwide?

Women die as a result of complications during and following pregnancy and childbirth. Most of
these complications develop during pregnancy and most are preventable or treatable. Other
complications may exist before pregnancy but are worsened during pregnancy, especially if not
managed as part of the woman’s care. The major complications that account for nearly 75% of all
maternal deaths are:

severe bleeding (mostly bleeding after childbirth)

infections (usually after childbirth)
high blood pressure during pregnancy (pre-eclampsia and eclampsia)
complications from delivery

The remainder are caused by or associated with infections such as malaria or related to chronic
conditions like cardiac diseases or diabetes.

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Why do women die in Pregnancy and Childbirth in the United

States?

Compare the data that you learned about above with percentages of pregnancy-related deaths in the
United States during 2014–2017.

Other cardiovascular conditions, 15.5%.

Infection or sepsis, 12.7%.
Cardiomyopathy, 11.5%.
Hemorrhage, 10.7%.
Thrombotic pulmonary or other embolism, 9.6%.
Cerebrovascular accidents, 8.2%.
Hypertensive disorders of pregnancy, 6.6%.
Amniotic fluid embolism, 5.5%.
Anesthesia complications, 0.4%.
Other noncardiovascular medical conditions, 12.5%.

The cause of death is unknown for 6.7% of all 2014–2017 pregnancy-related deaths.

While the contributions of hemorrhage, hypertensive disorders of pregnancy (i.e., preeclampsia,

eclampsia), and anesthesia complications to pregnancy-related deaths have declined, the
contributions of cardiovascular, cerebrovascular accidents, and other medical conditions have
increased.12 Studies show that an increasing number of pregnant women in the United States have
chronic health conditions such as hypertension,13,14 diabetes,14-17 and chronic heart
disease.12,18 These conditions may put a woman at higher risk of complications during pregnancy or
in the year postpartum.

Miscarriage

Pregnancy loss is experienced in an estimated 20-40 percent of undiagnosed pregnancies and in

another 10 percent of diagnosed pregnancies. Usually, the body aborts due to chromosomal
abnormalities and this typically happens before the 12th week of pregnancy. Cramping and bleeding
result and normal periods should return after several months. Or it may be necessary to have a
surgical procedure called D&E (dilation and evacuation). Some women are more likely to have

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repeated miscarriages due to chromosomal, amniotic, or hormonal problems; but miscarriage can
also be a result of defective sperm (Carroll et al., 2003).

In the U.S., a pregnancy loss before the 20th week of pregnancy is referred to as a miscarriage,
while the term stillbirth refers to the loss of a baby after 20 weeks’ gestation. A woman must still
go through labor or a c-section to deliver her baby. Stillbirth affects about 1 in 160 births, and each
year about 24,000 babies are stillborn in the United States. That is about the same number of babies
that die during the first year of life and it is more than 10 times as many deaths as the number that
occur from Sudden Infant Death Syndrome (SIDS).

As you can see, what may seem like a simple process is in fact a beautiful and delicate journey.
Each pregnancy and birth story is unique and comes with surprises and sometimes challenges. As
medical technology has rapidly improved, women are empowered with more information and more
choices when it comes to their pregnancy and birth. However, just because interventions are
available does not mean that this is the path for all mothers. As we learned in the case with Serena
Williams, even in the U.S. sometimes medical care can go awry. Each mother needs to be an active
advocate for herself and her baby during her pregnancy and delivery.

Where do you think we are headed with how medical advances are used in pregnancy and delivery?
More women are able to get pregnant with reproductive assistance, oftentimes past the age that they
would naturally conceive. At the beginning of the module, the topic of “designer babies” was
introduced. After completing this module, do you think that we are headed towards this in the near
future? What are the ethical ramifications?

Additional Supplemental Resources

Websites

The Human Genome Project (Links to an external site.)

The Human Genome Project (HGP) was an inward voyage of discovery led by an
international team of researchers looking to sequence and map all of the genes — together
known as the genome — of members of our species, Homo sapiens. Beginning in October

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1990 and completed in April 2003, the HGP gave us the ability, for the first time, to read
nature’s complete genetic blueprint for building a human being.
Institute for Behavioral Genetics (Links to an external site.)
Founded in 1967, IBG is one of the top research facilities in the world for genetic research
on behavior. Data collection and analysis are ongoing for several internationally renowned
studies including the Colorado Adoption Project, the Colorado Twin Registry, the
National Youth Survey Family Study, the Colorado Learning Disabilities Research Center,
and the National Longitudinal Study of Adolescent Health.

Videos

Fertilization
This video, created by Nucleus Medical Media, shows human fertilization, also known as
conception. Shown at a cellular level magnification, sperm struggle through many
obstacles in the female reproductive tract to reach the egg. Then genetic material from the
egg and a single sperm combines to form a new human being.
Conception to birth- Visualized
Image-maker Alexander Tsiaras shares a powerful medical visualization, showing human
development from conception to birth and beyond.
What are DNA and Genes?

The Genetic Science Learning Center sponsored by the University of Utah delivers
educational materials on genetics, bioscience, and health topics. All humans have the
same genes arranged in the same order. And more than 99.9% of our DNA sequence is the
same. But the few differences between us (all 1.4 million of them!) are enough to make
each one of us unique.
What is Inheritance?
The Genetic Science Learning Center sponsored by the University of Utah delivers
educational materials on genetics, bioscience, and health topics. This video explains the
importance of genetic variation.
Down Syndrome- Ability Awareness
What comes to mind when you think of a person who has Down Syndrome? Do you have
a preconceived idea of what their abilities might be? Chris Burke talks about his

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experience and his work at the National Down Syndrome Society.

Prenatal Testing Options
The University of Michigan provides this video that explains the difference between
prenatal screening and diagnostic testing. Pregnant women are faced with the decision of
whether to undergo prenatal screening and testing – and, if so – which of the many
options to choose from.
Prenatal Development: What We Learn Inside the Womb
Let’s watch what we experience and learn inside the womb from the fetus’ perspective.
TED talk: How CRISPR lets us Edit our DNA
Geneticist Jennifer Doudna co-invented a groundbreaking new technology for editing
genes, called CRISPR-Cas9. The tool allows scientists to make precise edits to DNA
strands, which could lead to treatments for genetic diseases … but could also be used to
create so-called “designer babies.” Doudna reviews how CRISPR-Cas9 works — and asks
the scientific community to pause and discuss the ethics of this new tool.

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