Lifespan Development Flashcards
What is reaction range, and an example?
A range of reaction for certain traits dependent on environmental factors. ‘Canalization’ refers to characteristics in which genotype restricts phenotype to a small number of possible outcomes.
Passive genotype-environment correlation
Children inherit traits from their parents that predispose them to particular traits and then their environment reinforces them (e.g., athleticism)
Evocative genotype-environment correlation
Child’s genetic makeup evokes reactions from parents which then reinforces it
Active genotype-environment correlation
Also referred to as ‘niche-picking’
Children seek out experiences that are consistent with genetic predispositions
This becomes more important as children become more independent
Epigenesis
Gene-environment interactions relative to developmental stage
Critical periods versus sensitive periods
Critical periods - specific, predetermined periods of time during biological maturation when an organism is sensitive to specific stimuli that can impact development
Sensitive periods - longer in duration than critical periods, more relevant to human development, not tied to chronological/maturational age
Bjorkhund and Pellegrini
Prolonged juvenile period evolved because humans require an extended period of time to develop a large brain. Childhood behaviors prepare children for adulthood.
Ontogenic adaptations
Childhood behaviors that are adaptive at specific points in development
Stages of prenatal development
Germinal stage - first 2 weeks when the fertilized ovum becomes a zygote
Embryonic stage - third week to the eighth eek
Fetal stage - onset of the nineth week until birth
Chromosomes
Human cells contain 46 chromosomes arranged into 23 pairs.
22 are autosomes
The 23rd is a sex chromosome.
Phenylketonuria (PKU)
A recessive gene disorder
People with PKU do not produce an enzyme used to metabolize phenylalanine which is an amino acid found in foods.
Requires people to start a low phenyl… diet early in life to stave of ID
Dominant gene disorders
Inheritance of a single dominant gene from one parent
Ex. Huntington’s disease
Recessive gene disorders
Inheritance of recessive genes, one from each parent
Ex. sickle cell, Tay sachs, cystic fibrosis
Chromosomal disorders
Variation in the number of chromosomes (aneuploidy) - Downs, Klinefelters, Turner and an alteration in their structure
Down syndrome
Extra chromosome 21
Characterized by ID, distinctive physical features, increased risk for AD, leukemia, and heart defects
Risk for DS increases as parental age increases
Klinefelter syndrome
Occurs in males due to the presence of 2 X chromosomes and 1 Y chromosome
Characterized by small penis and testes, breasts at puberty, limited interest in sex, sterility, learning disabilities
Turner syndrome
Occurs in females
Presence of a single X chromosome
Short, drooping eyelids, webbed neck, slow or absent secondary sex characteristics, cognitive deficits
Chromosomal deletion
Part of a chromosome is missing
Prader-Willi syndrom - ID, obesity, OC behaviors
Chromosomal translocation
Transfer of a chromosome segment to another chromosome
Can occur in Down syndrom
Chromosomal inversion
When a chromosome breaks in 2 places and forms inverts and then re-attaches
Can be inherited, do not typically impact phenotype
Fetal Alcohol syndrome
FAS is the most severe form - occurs when mother drinks heavily nearly every day or binge drinks in the second half of the first trimester
Associated with facial abnormalities, heart/kidney/liver defects, behavioral problems, vision and hearing problems
Alcohol-related neurodevelopmental disorder (ARND)
Cognitive deficits and behavioral problems without prominent facial anomalies
Alcohol-related birth defects
Involves physical defects without other prominent symptoms
Brain regions affected by FASD
corpus callosum, hippocampus, hypothalamus, cerebellum, basal ganglia, frontal lobes