Development: A continuous, biological process of modification and change — not isolated events.
Prenatal period: Conception to birth.
Postnatal period: Birth to death.
Milestones like childhood or adolescence are convenient markers but are part of a seamless process.
Chapter focus:
Development from conception through prenatal period.
Birth process.
Postnatal developmental changes.
Effects of aging on body systems.
Begins at fertilization (union of sperm and ovum).
Lasts ~ 39 weeks until birth.
Study of prenatal development = Embryology.
Describes transformation from a single cell to a complex human.
Ovulation: Ovum released → pelvic cavity → uterine (fallopian) tube.
Fertilization:
Usually occurs in the outer one-third of the fallopian tube.
Produces a zygote: single cell with complete genetic info (sex, body build, skin color already determined).
Cell Stages:
Zygote undergoes mitosis.
~3 days later → solid mass of cells = morula.
Morula hollows out into blastocyst.
Implantation:
Blastocyst embeds into uterine lining ~10 days after fertilization.
Before placenta forms, nutrients come from uterine fluids.
Blastocyst structure: Outer layer + inner cell mass → forms yolk sac & amniotic cavity.
Yolk sac:
In humans, not for nutrition.
Functions: early blood cell production, stem cell formation for gonads.
Amniotic cavity:
Fluid-filled sac (“bag of waters”) cushions & protects embryo.
Chorion: Outer membrane → chorionic villi connect embryo’s blood supply to placenta.
Placenta:
Exchange of nutrients, wastes, gases.
Acts as respiratory, excretory, endocrine organ.
Protective placental barrier — prevents most mixing of maternal & fetal blood.
Not foolproof: Alcohol, CMV, Zika, syphilis can cross.
Gestation period: ~39 weeks → divided into three trimesters.
First trimester:
Zygote → morula → blastocyst → implantation.
Embryonic phase: Week 3–8 after fertilization.
By day 35: Heart beating, limbs forming.
Fetal phase: Week 9–birth.
End of 1st trimester: Fetus ~7–8 cm, limbs complete, gender visible.
By month 4: All organ systems formed and functioning.
Early embryonic cells = stem cells (unspecialized, can become any tissue).
Three primary germ layers:
Endoderm (inside) → digestive tract lining, respiratory lining, glands.
Mesoderm (middle) → muscles, bones, circulatory system, connective tissue.
Ectoderm (outside) → skin, nervous tissue.
These layers give rise to all specialized tissues and organs.
Definition: Fertilization in lab dish; part of assistive reproductive technologies (ARTs).
Classic method:
Ovum retrieved via laparoscopy.
Newer method: Needle guided by ultrasound through vaginal wall.
Ovum mixed with sperm → 2–5 days growth → implanted into uterus.
Genetics:
Screening possible before implantation.
Ethical debates over gender selection.
Histogenesis: Germ layers → tissues.
Organogenesis: Tissues → organs.
Development involves cell differentiation, multiplication, growth, apoptosis, rearrangement in set sequence.
By 4 months: All organ systems in place; after that → growth dominates.
Ectoderm: Epidermis, tooth enamel, lens/cornea, outer ear, nasal cavity, brain/spinal cord, adrenal medulla, pituitary gland.
Mesoderm: Dermis, circulatory system, kidneys, gonads, muscle, bones (except facial), adrenal cortex.
Endoderm: GI tract lining, lung lining, hepatic/pancreatic ducts, bladder lining, thymus, thyroid, parathyroid, tonsils.
Transition from prenatal to postnatal life.
Caused by uterine contractions + cervical dilation.
Amniotic sac rupture = “water breaking”.
Fetus fails to rotate head-down before delivery → buttocks or feet present first.
Can make vaginal delivery risky → often requires C-section.
Surgical delivery via abdominal & uterine incision.
Indications: Breech birth, fetal/maternal complications, inability to safely deliver vaginally.
Stage One: Onset of contractions → full cervical dilation.
Stage Two: Full dilation → delivery of baby.
Stage Three: Delivery of placenta (~15 min after baby).
Average = 266 days from conception, 280 from last menstrual period.
<37 weeks = premature; >42 weeks = postmature.
Red bars = high risk of major congenital conditions.
Yellow bars = risk of minor congenital conditions.
Most vulnerable period: Early embryonic development.
Cord blood rich in stem cells → can be stored for future treatments (e.g., leukemia).
Safer and more available than bone marrow stem cells.
Fetus positioned.
Amniotic sac ruptures; cervix dilates.
Full cervical dilation; sac rupture widens.
Baby delivered through birth canal.
Placenta expelled.
Identical (monozygotic) twins:
One zygote splits early → genetically identical.
Usually share placenta, have separate cords.
Same genetic code, but can differ due to environment.
Fraternal (dizygotic) twins:
Two ova fertilized by different sperm.
Genetically like siblings.
Separate placenta & amnion.
Fertility treatments ↑ likelihood of multiple births.
What is the postnatal period? The prenatal period?
Postnatal period: Begins at birth and continues until death.
Prenatal period: Begins at conception (fertilization) and ends at birth.
What is a zygote? How is it different from a morula or blastocyst?
Zygote: Single-celled organism formed at fertilization, containing the complete genetic code.
Morula: Solid mass of cells formed after several divisions of the zygote (~3 days).
Blastocyst: Hollow ball of cells formed from the morula before implantation.
Name and describe the three primary germ layers.
Endoderm: Inside layer; forms GI tract lining, lung lining, and some glands.
Mesoderm: Middle layer; forms muscles, bones, circulatory system, connective tissues.
Ectoderm: Outside layer; forms skin and nervous tissue.
What are stem cells?
Unspecialized cells capable of producing many different kinds of specialized cells.
What is meant by the term organogenesis?
The process by which tissues arrange themselves into organs.
How does a breech birth differ from a typical birth?
In breech birth, the fetus is positioned so that the buttocks or feet are delivered first instead of the head.
Name and describe the three stages of labor.
Stage One: Onset of contractions to full cervical dilation.
Stage Two: Full dilation to delivery of the baby.
Stage Three: Delivery of the placenta.
How do multiple births occur?
Identical twins: One zygote splits early in development → genetically identical offspring.
Fraternal twins: Two separate ova are fertilized by different sperm during the same menstrual cycle.
Fertility treatments can increase the chance of multiple births.
Identify the primary difference between identical and fraternal twins.
Identical twins share the same genetic code from one zygote; fraternal twins are genetically like regular siblings from two separate fertilizations.
What is an Apgar score?
A scoring system used after birth to evaluate a newborn’s heart rate, respiration, muscle tone, skin color, and response to stimuli.
A successful pregnancy depends on proper implantation of the blastocyst in the uterine wall.
Improper implantation can cause:
Ectopic pregnancy: Implantation outside the uterus (most often in a fallopian tube — tubal pregnancy). Tube can rupture → severe bleeding → life-threatening.
Placenta previa: Placenta grows too close to the cervical opening; may cause painless bleeding during late pregnancy, can endanger mother & baby.
Abruptio placentae: Complete separation of placenta from uterine wall before delivery → immediate fetal death and maternal hemorrhage.
Ectopic pregnancies often require C-section delivery.
Also called toxemia of pregnancy.
Serious condition in ~1 in 20 pregnancies after 24 weeks.
Characterized by:
High blood pressure.
Proteinuria.
Edema.
Can cause abruptio placentae, stroke, hemorrhage, fetal malnutrition, low birth weight.
May progress to eclampsia → seizures, coma, organ failure, possibly death.
High blood glucose first detected during pregnancy.
Caused by pregnancy hormones promoting insulin resistance.
Can occur in women with undiagnosed type 1 or type 2 diabetes.
Risks:
Large infant size → difficult delivery or need for C-section.
Increased risk of preeclampsia.
Can harm both mother and fetus if uncontrolled.
Miscarriage (spontaneous abortion): Loss before 20 weeks (<500 g or 1.1 lb).
Stillbirth: Death after 20 weeks gestation.
Causes: Hypertension, uterine conditions, hormonal imbalances, structural/genetic abnormalities.
Developmental problems present at birth — structural, functional, or behavioral.
Causes:
Genetic factors (inherited mutations, chromosomal abnormalities).
Teratogens — environmental agents causing defects:
Radiation (x-rays).
Toxic chemicals (drugs, cigarette smoke, alcohol).
Infections in mother (herpes, Zika, CMV).
Nutritional deficiencies.
Highest risk period = First trimester during organ differentiation.
Severe damage can cause miscarriage.
Puerperal fever (childbed fever):
Bacterial infection post-delivery.
Historically a major cause of maternal death; now rare with antibiotics.
Lactation needs: Breastfeeding important for newborn nutrition.
Mastitis: Inflammation/infection of breast tissue → possible milk contamination.
Lactose intolerance in infants: Caused by lack of lactase enzyme → may need lactose-free formula.
Antenatal medicine: Diagnosis & treatment before birth.
Includes:
Ultrasound (ultrasonogram) — 2D/3D imaging.
Prenatal surgery (e.g., bladder repair).
Monitoring fetal health.
Treating conditions like Rh incompatibility before birth.
Caused by alcohol crossing placenta into fetal circulation.
Effects:
Microcephaly (“small head”).
Low birth weight.
Developmental & learning disabilities.
Growth restrictions.
Facial abnormalities.
Possible fetal death.
Even small amounts of alcohol in pregnancy can cause harm.
What conditions can result from improper implantation in the uterine wall?
Ectopic pregnancy, placenta previa, abruptio placentae.
What complications may occur as a result of preeclampsia?
Abruptio placentae, stroke, hemorrhage, fetal malnutrition, low birth weight, and possible progression to eclampsia.
What is a teratogen? Give some examples.
An agent causing developmental defects; examples: radiation, toxic chemicals (drugs, alcohol), infections (herpes, Zika, CMV).
What is gestational diabetes?
Diabetes first diagnosed during pregnancy, caused by insulin resistance; can harm both mother and baby.
Begins at birth, lasts until death.
Divided into major periods: infancy, childhood, adolescence, adulthood, older adulthood.
Growth & development involve continuous changes in body proportions and structure.
Infant’s head ≈ 1/4 of total height; adult’s head ≈ 1/8.
Face: infant’s face ≈ 1/8 of head; adult’s ≈ 1/2 of head.
Legs grow proportionately longer, trunk proportionately shorter.
Trunk shape changes from round → more elongated.
From birth to 18 months.
First 4 weeks = neonatal period.
Neonatology: medical specialty for newborns.
Cardiovascular & respiratory system changes critical at birth (first breath triggers lung function).
Birth weight doubles by 4 months, triples by 1 year.
“Baby fat” peaks then declines; infant becomes leaner.
Spinal curves: At birth only one curve; cervical curve appears by 3–4 months; lumbar curve appears by 12–18 months → toddler can stand/walk.
Milestones:
Follow object with eyes (2 months)
Lift head/chest (3 months)
Sit (6 months)
Stand (12 months)
Run (18 months)
End of infancy to puberty (12–14 years girls, 14–16 boys).
Rapid growth but less consistent month-to-month.
Deciduous teeth lost ~age 6; permanent teeth erupt, including wisdom teeth by ~age 14.
Teenage years (13–19).
Physical growth → sexual maturity.
Controlled by sex hormones; secondary sex characteristics develop.
Girls: breast development first sign; menarche ~12–13 years.
Boys: testicular enlargement 10–13 years; both sexes have height growth spurts (girls ~10–12, boys ~12–13).
Maturation continues (bone closure, organ placement changes).
Maintenance of body tissues is main process.
With age, repair becomes harder → degeneration begins.
Peak function early, then gradual decline in all systems.
Gerontology = study of aging.
Figure 24-15 shows % of function remaining in older adult organs vs. 20-year-old:
Brain weight: 85%
Cardiac output: 65%
Respiratory capacity: 55%
Kidney mass: 85%
Liver blood flow: 50%
Hutchinson-Gilford syndrome: rare, non-inherited genetic condition.
Rapid aging due to excess progerin protein.
Symptoms: thin skin, hair loss, stiff joints, loss of subcutaneous fat.
Death usually from cardiovascular disease by ~14 years.
Senescence = degenerative changes with age.
Hypotheses:
Telomere shortening: cells can only divide ~50 times.
Apoptosis: programmed cell death increases.
Free radical theory: reactive oxygen damages cells, antioxidants may help.
Autoimmunity: immune system attacks own tissues.
Aging rates vary among individuals due to genetics & environment.
Do the proportions of the human body change during postnatal development?
Yes; head becomes proportionately smaller, legs longer, trunk proportion changes.
What is the neonatal period of development?
The first 4 weeks of infancy after birth.
What biological changes happen during puberty?
Development of secondary sex characteristics, reproductive maturity, rapid physical growth.
What is senescence?
The process of aging marked by degenerative changes in body systems.
What are free radicals, and what role do they have in the aging process?
Reactive oxygen molecules that damage cells and contribute to aging.
Senescence = the degenerative changes of older adulthood.
Exact causes aren’t fully known. Key hypotheses in the text:
Cell‑division limit / telomeres: human cells can’t divide indefinitely; telomeres at chromosome ends shorten with each division and eventually cells stop dividing.
Apoptosis: continual programmed cell death; in older adulthood, dead cells may not be replaced → tissue degeneration.
Autoimmunity: immune system sometimes attacks the body’s own tissues in aging.
Preprogrammed/“aging genes” idea: genes may make aging “preprogrammed.”
Free‑radical theory: reactive oxygen species from normal cellular activity damage cells and promote aging; antioxidants may offer some protection.
Figure 24‑16: Loss of bone mineral density (BMD) in late adulthood → spinal curvature changes and shortened stature.
Becomes dry, thin, and inelastic (“sags”); wrinkles and skin folds increase.
Pigmentation changes; thinning or loss of hair are common.
Bones change in texture, degree of calcification, and shape with age.
Edges of older bones look indistinct/shaggy with spurs—called lipping—which restricts movement by building up around joints.
Reduced calcification → smaller bones, porous bones → fracture risk.
Lower cervical & thoracic vertebrae fracture frequently → spine curvature + shorter stature (links to Fig. 24‑16).
Degenerative joint disease (osteoarthritis) is common, but exercise started earlier in life lessens many changes.
Exercise also helps offset bone mass loss when paired with good nutrition.
Skeletal muscle mass declines with age: may start ~age 25, usually not reaching 10% loss until ~50.
By ~80, many have lost ≈50% of skeletal muscle mass.
Weight training before and during later years can increase remaining fiber size and counteract some loss in fiber number.
Risk of dementia (loss of memory/other conscious thinking functions) increases.
For most, memories remain mostly intact, with mature reasoning/decision‑making.
Some experience depression (especially with illness or separation), but on average older adults are happier than in early/middle adulthood.
Vision:
By ~65, lenses become hard and lose elasticity → presbyopia (can’t accommodate for near vision).
Many notice near‑vision difficulty at 40–45 → need bifocals/mixed‑focus lenses.
Lens loses transparency → cataract (clouding) requiring surgical removal.
Glaucoma incidence rises with age (↑ intraocular pressure); untreated, can cause blindness; risk of retinal degeneration/detachment also ↑ with age.
Hearing:
Significant loss of hair cells in the spiral organ; eardrum/ossicles stiffen → poorer sound transmission; hearing impairment is nearly universal in older adults.
Taste & Smell:
Both decrease; only ~40% of taste buds present at age 30 remain by 75.
Degenerative heart & vessel disease is common/serious.
Atherosclerosis (fatty deposits in vessel walls) → narrowed lumens → coronary artery disease and myocardial infarction.
Arteriosclerosis = hardening of arteries; rupture can cause stroke (CVA).
Hypertension (HTN) more common; stiff arteries raise systolic pressure.
Costal cartilages harden/calcify → rib cage less able to expand/contract; may become fixed to sternum → “barrel chest.”
Respiratory efficiency decreases.
Atrophy of respiratory muscles + replacement by connective tissue → weaker inspiration/expiration.
Functioning nephron units decrease by ~50% between ages 30 and 75.
Renal blood flow decreases → ↓ renal function and excretory capacity (and ability to produce urine).
Bladder muscle atrophies → incontinence & trouble emptying/voiding completely.
General: many remain sexually active; response patterns change, and fertility declines.
Males: erection may be harder to achieve/maintain; urgency for sex may decline, possibly from reduced testosterone (“low T”). Some develop andropause when testosterone falls enough to cause infertility.
Females: typical cessation of reproductive cycling 45–60 → menopause due to decreased estrogen.
Symptoms: hot flashes, sleep disturbances, dryness & thinning of the vaginal wall.
↓ estrogen is tied to bone loss/osteoporosis (see Ch. 8).
Hormone replacement therapy (HRT/HT) used in the past; more cautious now due to increased risks (some cancers, stroke, blood clots), though still used individually.
Non‑estrogen meds also available to manage symptoms and other problems (e.g., bone loss, heart disease).
Better food, safer surroundings, and advanced medical care have extended quality living.
Low‑tech lifestyle keys that most people can do:
Eat a healthful diet
Exercise (even light/moderate) — keeps skeletal/muscular systems fit and decreases aging’s effects on several systems
Manage stress (even meditation and tai chi help)
Bottom line: we can often stay “young” longer if we eat right, exercise, and relax.
CONNECT IT!: Notes the role of genes in longevity (see “Genes and Longevity”).
Rita Levi‑Montalcini (1909–2012):
Early lab work led to discovery of nerve growth factor (NGF); awarded the 1986 Nobel Prize.
Her work on growth regulators deepened understanding of nervous system development and other tissues/organs.
Impact beyond prenatal care: insights from embryology now inform gerontology (study of aging) and geriatrics (care of the aged), including possibilities to repair/regenerate damaged tissues in older adults.
Skeletal changes with age?
Bone texture/calcification/shape change; lipping around joints; smaller, porous bones; frequent vertebral fractures → spinal curvature & shorter stature; osteoarthritis common.
Eyesight in late adulthood?
Presbyopia (stiff lens); need for bifocals; ↑ risk of cataracts and glaucoma; reduced lens transparency.
Cardiovascular changes in older adults?
Atherosclerosis/arteriosclerosis, ↑ risk of MI and stroke; hypertension more common as arteries stiffen.
Kidney function in old age?
≈50% fewer nephrons (30→75 yrs) + ↓ renal blood flow → ↓ renal function and excretory capacity; bladder muscle atrophy → incomplete emptying/incontinence.