Module 3 Fetal Development
Module 3 Fetal Development
3 FETAL DEVELOPMENT
Learning Objectives
By the end of this section, you will be able to:
1. Differentiate between the embryonic period and the fetal period
2. Briefly describe the process of sexual differentiation
3. Describe the fetal circulatory system and explain the role of the shunts
4. Trace the development of a fetus from the end of the embryonic period to birth
As you will recall, a developing human is called a fetus from the ninth week of gestation until
birth. This 30-week period of development is marked by continued cell growth and
differentiation, which fully develop the structures and functions of the immature organ systems
formed during the embryonic period. The completion of fetal development results in a newborn
who, although still immature in many ways, is capable of survival outside the womb.
SEXUAL DIFFERENTIATION
Sexual differentiation does not begin until the fetal period, during weeks 9–12. Embryonic males
and females, though genetically distinguishable, are morphologically identical. Bipotential
gonads, or gonads that can develop into male or female sexual organs, are connected to a central
cavity called the cloaca via Müllerian ducts and Wolffian ducts. (The cloaca is an extension of
the primitive gut.) Several events lead to sexual differentiation during this period.
During male fetal development, the bipotential gonads become the testes and associated
epididymis. The Müllerian ducts degenerate. The Wolffian ducts become the vas deferens, and
the cloaca becomes the urethra and rectum.
During female fetal development, the bipotential gonads develop into ovaries. The Wolffian
ducts degenerate. The Müllerian ducts become the uterine tubes and uterus, and the cloaca
divides and develops into a vagina, a urethra, and a rectum.
THE FETAL CIRCULATORY SYSTEM
During prenatal development, the fetal circulatory system is integrated with the placenta via the
umbilical cord so that the fetus receives both oxygen and nutrients from the placenta. However,
after childbirth, the umbilical cord is severed, and the newborn’s circulatory system must be
reconfigured. When the heart first forms in the embryo, it exists as two parallel tubes derived
from mesoderm and lined with endothelium, which then fuse together. As the embryo develops
into a fetus, the tube-shaped heart folds and further differentiates into the four chambers present
in a mature heart. Unlike a mature cardiovascular system, however, the fetal cardiovascular
system also includes circulatory shortcuts, or shunts. A shunt is an anatomical (or sometimes
surgical) diversion that allows blood flow to bypass immature organs such as the lungs and liver
until childbirth.
The placenta provides the fetus with necessary oxygen and nutrients via the umbilical vein.
(Remember that veins carry blood toward the heart. In this case, the blood flowing to the fetal
Figure2Fetal
OTHER ORGAN SYSTEMS
During weeks 9–12 of fetal development, the brain continues to expand, the body elongates, and
ossification continues. Fetal movements are frequent during this period, but are jerky and not
well-controlled. The bone marrow begins to take over the process of erythrocyte production—a
task that the liver performed during the embryonic period. The liver now secretes bile. The fetus
circulates amniotic fluid by swallowing it and producing urine. The eyes are well-developed by
this stage, but the eyelids are fused shut. The fingers and toes begin to develop nails. By the end
of week 12, the fetus measures approximately 9 cm (3.5 in) from crown to rump.
The fetus continues to lay down subcutaneous fat from week 31 until birth. The added fat fills
out the hypodermis, and the skin transitions from red and wrinkled to soft and pink. Lanugo is
shed, and the nails grow to the tips of the fingers and toes. Immediately before birth, the average
crown-to-rump length is 35.5–40.5 cm (14–16 in), and the fetus weighs approximately 2.5–4 kg
(5.5–8.8 lbs). Once born, the newborn is no longer confined to the fetal position, so subsequent
measurements are made from head-to-toe instead of from crown-to-rump. At birth, the average
length is approximately 51 cm (20 in).
The passage of meconium in the uterus signals fetal distress, particularly fetal hypoxia (i.e.,
oxygen deprivation). This may be caused by maternal drug abuse (especially tobacco or
cocaine), maternal hypertension, depletion of amniotic fluid, long labor or difficult birth, or a
defect in the placenta that prevents it from delivering adequate oxygen to the fetus. Meconium
passage is typically a complication of full-term or post-term newborns because it is rarely
passed before 34 weeks of gestation, when the gastrointestinal system has matured and is
appropriately controlled by nervous system stimuli. Fetal distress can stimulate the vagus
nerve to trigger gastrointestinal peristalsis and relaxation of the anal sphincter. Notably, fetal
hypoxic stress also induces a gasping reflex, increasing the likelihood that meconium will be
inhaled into the fetal lungs.
Although meconium is a sterile substance, it interferes with the antibiotic properties of the
amniotic fluid and makes the newborn and mother more vulnerable to bacterial infections at birth
and during the perinatal period. Specifically, inflammation of the fetal membranes, inflammation
of the uterine lining, or neonatal sepsis (infection in the newborn) may occur. Meconium also
irritates delicate fetal skin and can cause a rash.
The first sign that a fetus has passed meconium usually does not come until childbirth, when the
amniotic sac ruptures. Normal amniotic fluid is clear and watery, but amniotic fluid in which
meconium has been passed is stained greenish or yellowish. Antibiotics given to the mother
may reduce the incidence of maternal bacterial infections, but it is critical that meconium is
aspirated from the newborn before the first breath.
Aspiration of meconium with the first breath can result in labored breathing, a barrel-shaped
chest, or a low Apgar score. An obstetrician can identify meconium aspiration by listening to the
lungs with a stethoscope for a coarse rattling sound. Blood gas tests and chest X-rays of the
infant can confirm meconium aspiration. Inhaled meconium after birth could obstruct a
newborn’s airways leading to alveolar collapse, interfere with surfactant function by stripping it
from the lungs, or cause pulmonary inflammation or hypertension. Any of these complications
will make the newborn much more vulnerable to pulmonary infection, including pneumonia.
CHAPTER REVIEW
The fetal period lasts from the ninth week of development until birth. During this period, male
and female gonads differentiate. The fetal circulatory system becomes much more specialized
Review Questions
1. The foramen ovale causes the fetal circulatory system to bypass the ________.
A. liver
B. lungs correct answer
C. kidneys
D. gonads
2. What happens to the urine excreted by the fetus when the kidneys begin to function?
1. What is the physiological benefit of incorporating shunts into the fetal circulatory system?
Circulatory shunts bypass the fetal lungs and liver, bestowing them with just enough
oxygenated blood to fulfill their metabolic requirements
2. Why would a premature infant require supplemental oxygen? chronic lung disease
GLOSSARY
1. ductus arteriosus
3. foramen ovale
shunt that directly connects the right and left atria and helps divert oxygenated blood
from the fetal pulmonary circuit
4. lanugo
silk-like hairs that coat the fetus; shed later in fetal development
5. meconium
fetal wastes consisting of ingested amniotic fluid, cellular debris, mucus, and bile
6. quickening
fetal movements that are strong enough to be felt by the mother
7. shunt
circulatory shortcut that diverts the flow of blood from one region to another
8. vernix caseosa
waxy, cheese-like substance that protects the delicate fetal skin until birth