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POINTERS TO REVIEW IN EDUC 102 Fraternal twins (dizygotic)

Genetic and Chromosomal Abnormalities Stages of Prenatal Period


1. Germinal Stage

 Some are known as early as birth while others Cell division begins approximately 24-36 hours after
conception
appear later in life
Morula (3-4 days after fertilization)
 Studies have shown that there are more than
4000 Blastocyst (4-5 days after fertilization)

human genetic disorder which either caused by As cells multiply, they will separate into two distinctive
masses
recessive gene and dominant gene
Placenta – outer cells
 Genetics plays a major role in development.
Embryo – inner cells
However, in some cases genetic problems can
Blastocyst
emerge that may impact both current and future
• Endoderm – inner layer (which will become the
development digestive and respiratory system)
Down Syndrome • Mesoderm – middle layer (which will become the
muscle and skeletal system)
 also known as trisomy 21
 The most common genetic abnormality during • Ectoderm – outer layer (which will become the skin
prenatal development which is caused by an and nervous system)
extra
Implantation – happens when the blastocyst arrives at
chromosome on the 21st pair (there are 3 chromosomes the uterus and attached to the uterine wall When
instead of the usual 2) implantation is successful, hormonal changes halt a
woman’s normal menstrual cycle and cause a whole host
 Typical features include flattened facial features, of physical changes
heart defects and intellectual disability Teratogen - substances or diseases that can cause birth
Inherited diseases defect
Kinds of Birth
 A number of illness can be inherited if one or
both Natural Childbirth- refer to vaginal labor and delivery
with limited to no medical intervention
parents carry a gene for the disease
Caesarean Delivery (C-section)- may be necessary for
 Genetic tests can often determine if a parent is a
the safety of expectant mother and the baby, especially
carrier of genes for a specific disease when one of these complications is present ;

Sex-Chromosomal Abnormalities • When the baby is not in the head-down position

1. Klinefelter’s syndrome – when a boy is born • When the baby is too large to pass through the
with an extra copy of the X chromosomes; also
pelvis
known as 47 or XXY
2. Turner syndrome – chromosomal condition • When the baby is in distress
that affects the development in females; missing
one of their X chromosomes APGAR

Sex Determination in Human Being Appearance (skin color)

The twenty-third pair consists of sex chromosomes Pulse

Multiple Births Grimace (reflex irritability)

Identical twins (monozygotic) Activity


Respiration 3. Night time urination (bed wetting) is the hardest for
Neonatal Reflexes young children to control
essential for a newborn's survival
Moro Reflex- outstretching of the arms and legs in BIOLOGICAL THEORY
response to a loud noise or sudden change in the
environment Explained children’s development in terms of innate
biological processes
Sucking Reflex- occurs when an object touches the lips
Heredity plays an important role in growth and
Rooting Reflex- turning of an infant’s head toward a development of the individual
stimulus such as a breast or hand
Genes – hereditary factor that carry the traits that were
Grasping Reflex (Palmar Grasp)- vigorous grasping of contributed by the parents
an object that touches the palm
DNA – (Deoxyribonucleic acid) a molecule composed of
Stepping (or Walking) Reflex- moves legs when held two chains that coil around each other to form a double
upright with feet touching the floor helix carrying the genetic instructions used in the
growth, development, functioning, and reproduction of
Tonic Neck Reflex- the arm on the side extends while all known living organisms and many viruses.
the opposite arm bends at the elbow (fencing position)
Chromosomes – a threadlike structure of nucleic acids
Babinski Reflex- outward projection of the big toe and and protein found in the nucleus of most living cells,
fanning of the others when the sole of the foot is touched carrying genetic information in the form of genes.
Motor Development Genotype – determine the features or trait of an
Gross Motor Development- require the coordination of organism
the large muscle groups of the body, such as the arms, Allele – variants of a gene
legs, and trunk
(Dominant and Recessive Allele)
Fine Motor Development- concerned with the
coordination of the smaller muscles of the body Homozygous – contain two identical alleles
including hands and face
Heterozygous – two alleles are different
Two Principles of Physical/Motor Development
Phenotype – expression of the genotype; depends on a
complex interaction between genes and the environment
Cephalocaudal Law – Children’s muscle control
develop from head to toe direction Polygenic traits – influenced by multiple genes
interacting with the environment in complex ways
Proximodistal Law – Children develop their motor
skills from the center of their bodies outward Dominant traits – traits that are passed on from
generation to generation; appeared in all first generation
Toilet Training offspring
Most children are toilet trained by the age 5 or 6 Recessive traits – appeared in about 1-quarter of the
second generation offspring
Children normally master toilet training tasks in a
specific Punnett Square
developmental order – devised by Reginald C. Punnett
1. Learn to notice the warning signals and react in time – used to predict the possible
to
genotypes of an offspring that may affect the expression
master daytime defecation and then night time of the phenotype
defecation
Gregor Mendel – Father of Genetics
2. Learn how to react to their bodies’ signals for daytime
• He formulated three laws that explain how traits are
urination transferred from generation to generation
Law of Dominance – the presence of one dominant gene
may mask or prevent the expression of recessive gene.
Law of Segregation – a pair of genes is separated during
the formation of gametes with every independent trait or
characteristics developing
Law of Independent Assortment – the separation of
gene pairs on a given pair of chromosomes and the
distribution of the genes during meiosis are entirely
independent of the distribution of other gene pairs on the
other pair of chromosomes. Each trait can hence be
paired with the other trait in the pair.
ECOLOGICAL THEORY
• Urie Bronfenbrenner (1917-2005)
• some systems help human development
Microsystem – locale in which the individual lives; help
shape the individual (family, peers, neighbourhood)
Mesosystem – relationship between and among the parts
of microsystem
Exosystem – includes the other people and places the MATURATION THEORY
individual may not interact with but still has a large • The maturation theory was introduced in 1925 by the
effect American psychologist Arnold Lucius Gesell, who was
Macrosystem – Most distant set of people but still has a also a pediatrician and educator.
great influence • The studies carried out by Gesell focused on finding
Chronosystem – result of the individual’s experience in out how development occurred during childhood and
his life; includes the transitions and shifts in one's adolescence, both in children without any
lifespan. This may also involve the sociohistorical psychopathology or those who showed a different
contexts that may influence a person. pattern of learning and development than expected.
• According to their theory of maturation, all children go
through the same stages of development in the same
order but not necessarily presenting them at the same
time. That is, each child goes at their own pace, but the
expected thing is that they do the learning in the same
sequence.

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