Child (0-12)
Teenager (13-19)
Twentysomething (20-29)
Thirtysomething (30-39)
Fortysomething (40-49) (formerly also Quadragenarian, rarely
used since 1980)
Quinquagenarian (50-59)
Sexagenarian (60-69)
Septuagenarian (70-79)
Octogenarian (80-89)
Nonagenarian (90-99)
Centenarian (100-109)
Supercentenarian (110+)
Fertilization occurs at
the time of conception
when the sperm cell
fertilizes the ovum
Process of Reproduction
Mature sex cells or
Gametes
Male: Sperm
forms
Zygote or
Fertilized Egg
Fallopian Tube
zygote goes
Womb or Uterus
Significant Events
During Conception
1. Heredity:
transmission of traits from
parents to offspring through the
genes
Biological inheritance
takes place during fertilization
Fertilization
2. Sex/ Gender:
Of the 23 pairs, 22 pairs called the
autosomes are of the same size and
shape
Sex is determined by the 23rd pair of
chromosomes known as the sex
chromosomes
Recessive Traits
Blue eyes
Straight hair
All types of hair
Normal/ fair
Normal hair color
Lack of dimples
Five fingers
Normal chin
Prenatal Development
Period of the Zygote/ Germinal Period:
Fertilization to end second week
Zygote is about the size of a pinhead
After 10 days, the zygote is implanted in
the uterine wall
3rd month
Digestive organs begin functioning
Bone formation
Sex organs develop rapidly
Arms, legs and fingers make spontaneous
movements
4th month
Face acquires human appearance
Lower body grows rapidly, outgrows the head
Most bones are distinctly seen
7th month
Fetus capable of living outside the uterus
Fetus looks like a dried up, aged person with
red, wrinkled skin
Cerebral fissures and convolutions develop
8th-9th months
Subcutaneous fat is deposited
Fingernail reach beyond fingertips
Hair is shed
Initial Myelination of the brain
Source: W. J. Robbins (1928) Yale University Press
Hazards
Physical conditions
Illnesses like rubella: risk of blindness, deafness,
brain damage, heart diseases
Maternal malnutrition: underweight at birth, may
suffer rickets, physical and neurological defects
Maternal age: teenage pregnancy may lead to
premature birth and undersized infants; a
healthy woman in her 30s and 40s may enjoy a
good prospect of giving birth with supervised
medical attention
Exposure to chemicals
Thalidomide (tranquilizer): malformed or
missing limbs
Quinine (for Malaria): congenital deafness
Barbiturates (sedatives): affects oxygen
supply and may cause brain damage
Antihistamine: spontaneous abortion
Caffeine: spontaneous abortion
Complications of delivery
Syphilis: fetal or perinatal death
Genital Herpes: infant may contract the
disease
HIV/ AIDS
Diabetes: stillborn, unformed spines,
misplaced heart, displaced hips
Rh Factor (incompatibility between mother
and infants blood): fatal anemia and
jaundice
Psychological Hazards
Traditional beliefs
Maternal Stress
Unfavorable attitude of significant others
Chromosomal
Aberrations
Downs Syndrome
Trisomy 21 (Down
Syndrome) is a genetic
disorder that occurs
when an extra copy of
the chromosome is
present in the 21st
chromosomal pairing.
The risk of carrying a
Trisomy 21 child
increases with age (after
35, the risk increases
dramatically).
Characteristics: mental
retardation, risk of heart
defects as well as
gastrointestinal problems
associated with intestine
or esophagus blockages.
Turner's Syndrome is a
relatively common disease in
females, affecting many body
systems.
Due to the deletion of the X
chromosome from the father
in the 23rd pair
Characteristics: short stature,
failure to mature sexually,
learning difficulties, skeletal
abnormalities, hearing loss,
liver dysfunction, heart and
kidney abnormalities, infertility,
and thyroid dysfunction
Turners
Syndrome
Trisomy 18 (Edwards
Syndrome) is a genetic
disorder that occurs when
an extra copy of the
chromosome is present in
the 18th chromosomal
pairing.
Majority of these children
die within a very short
time after birth. A higher
risk of the baby dying
whilst still in the uterus is
also a factor.
Mental retardation is an
inevitable result of this
extra chromosome.
Edwards Syndrome is
normally characterized by
low set ears, deformed
fingers, narrow nose and
a receding jaw as well as
congenital heart disease.
Edwards
Syndrome
Cri Du Chat
Syndrome is due to
a deletion of part of
chromosome 5.
The name is
derived from the
distinctive sound
made when
children with this
problem are crying
('Cri du Chat'
means 'Cat's Cry'
when translated
from French).
Characteristics:
distinctive facial
features, shortened
lifespan and suffer
varying levels of
mental retardation
Williams Syndrome
Due to a deletion of a part of
chromosome 7 occurs instead
of an extra copy of a
chromosome being present.
Characteristics: distinctive
facial features that appear
"elf-like" in appearance,
learning difficulties and a
loving/exuberant personality
is usual.
Medical problems associated
with Williams syndrome
include calcium instability,
artery anomalies, cardiac
problems and poor
conditioning of the
teeth/gums.
Cornelia de Lange
Due to a faulty
gene on
chromosome 3
Characteristics:
several physical
and
developmental
abnormalities.
Angelman Syndrome
Rare neurogenetic disorder
that is
predominantly
caused by
deletions on
chromosome 15
given by the
mother
Mostly of
Caucasian birth
Apert Syndrome
Duetogeneticmutation
onchromosome10
Characteristics:specific
craniofacialandlimb
abnormalities
Themutationcanbe
inheritedfromaparent
whohasApertsyndrome
oritcanbea
spontaneous(new)
mutation.
StudiesshowthatApert
syndrometendstooccur
moreofteninchildren
witholderfathers.
Klinefelters Syndrome
Due to an extra X chromosome
from the father on the 23rd pair
Characteristics: underdeveloped
secondary sex characteristics and
learning difficulties
Only occurs among males
References:
Balatbat, L., Entao, E. & Huvalla, C., (2004) Work text in
Fundamentals of Psychology, St. Scholasticas College.
Unpublished text book
Myers, David (1995) Psychology 4th ed. Worth
Publishers
National Center on Birth Defects and
Developmental Disabilities (2006) Center for Disease
Control and Prevention (2006) Fetal Alcohol Spectrum
Disorders. Date last retrieved: July 18, 2006.
http://www.cdc.gov/ncbddd/fas/fasask.htm
Vander Zanden, James (2000) Human
Development 7th ed. USA: McGraw-Hill (Revised by:
Thomas Crandell and Corrine Crandell