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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 ;
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