Life Span and Development Flashcards
What is the function of chromosomes
To carry hereditary traits children inherit from their parents
How many chromosomes are there
There are 46 total chromosomes
23 from the mother’s ovum
23 from the father’s sperm
What is a genotype
An individual’s complete genetic makeup, including traits in
recessive genes
What is a phenotype
An individual’s expressed characteristics (green eyes, red
hair)
What are carriers
Traits that are in our genotype but unexpressed as a
phenotype
What is a dominant-recessive trait
One gene pair is dominant and controls the trait.
The recessive gene is in the genotype but not part of the
phenotype
What are polygenic traits
Produced by interaction of many traits
What 2 things must happen to have a trait become a
Phenotype
2 levels of interaction must occur
1 Gene-Gene Interaction
2 Gene-Environment interaction
In a dominant-recessive pattern, what controls the trait
One gene pair is dominant and controls the trait
Recessive gene is in genotype, not part of phenotype
An example of dominant-recessive pattern is
Brown eyed father
Blue eyed mother (brown eye gene)
Hypothetically, 1 in 4 chance child will have blue eyes
3 in 4 chance children will have brown
Incomplete dominance
The phenotype is not completely controlled by the gene.
The gene does not completely control the trait
Where are X-linked genes located
On the X chromosomes
Where would a disease that is X linked be obtained from
The mother
Monozygotic twins occur when
One zygote splits and forms two identical clusters. Also
known as identical twins with identical genes
Dizygotic twins occur when
Two ova are fertilized by two separate sperm around the
same period
How often do Monozygotic births occur
About 1 in every 270 pregnancies
How often do Dizygotic births occur
About 1 in every 60 births
Chromosomal abnormalities are
When a baby is born with an abnormal number of
chromosomes 45, 47 or more. Occurs in 1 out of 200 births
Characteristics of Down syndrome
Involves an extra chromosome on the 21st pair
Has characteristics such as thick tongue, round face, slanted
eyes, short limbs, also slow to develop
Down syndrome
Is also known as trisomy 21. It is the most common
chromosomal abnormality
Involves an extra chromosome on the 21st pair
Characteristics: thick tongue, round face, slanted eyes, short
limbs, slow to develop
Phenylketonuria (PKU)
Involves abnormal ingestion of protein. Occurs in 1 out 500 births, 1 in 100 European Americans mainly of Norwegian decent It is caused by a recessive gene Can be prevented through diet Can be prenatally detected
Kleinfelter syndrome
Sufferers have an XXY chromosomal pattern
The individual has a seemingly male appearance, secondary
sex characteristics are not present
Fragile X syndrome
Involves part of the X chromosome attached thinly, ready to
break off.
Caused by mutated gene that contains A DNA sequence
CGG that is repeated 200 times, nl is 30
What are the domains of development
The biosocial domain includes brain, body changes and
influences that guide them
Cognitive, includes thought process, perceptual abilities,
language mastery
Psychosocial, includes personality, emotions, interpersonal
ie., family, friends