Chapter 2 - Genetic Bases of Childhood Development Flashcards
(29 cards)
Why do relatively few genetic disorders involve dominant alleles?
inherited disorders are rarely carried by dominant alleles because individuals with such a disorder usually don’t live long enough to have children
alleles
a variation of a specific gene
Define: sickle-cell trait
disorder in which individuals show signs of mild anemia only when they are seriously deprived of oxygen; occurs in individuals who have one dominant allele for normal blood cells and one recessive sickle-cell allele
Define: sex chromosomes
the 23rd pair of chromosomes; these determine the sex of the child
Define: recessive
an allele whose instructions are ignored when it is combined with a dominant allele
Define: polygenic inheritance
when phenotypes are the result of the combined activity of many separate genes
Define: phenotype
the physical, behavioural, and psychological features that are the result of the interaction between one’s genes and the environment
Define: niche-picking
the process of deliberately seeking environments that are compatible with one’s genetic makeup
Define: autosomes
the first 22 pairs of chromosomes, the chromosomes in each pair are about the same size
Define: behavioural genetics
the branch of genetics that deals with inheritance of behavioral and psychological traits
Define: chromosomes
tiny structures in the nucleus that contain genetic material
Define: deoxyribonucleic acid—DNA
a molecule composed of four nucleotide bases; the biochemical basis of heredity.
Define: dizygotic twins
twins from two separate eggs fertilized by two separate sperm, genetically, fraternal twins are just like any other siblings, on average, about half their genes are the same
Define: dominant
the form of an allele whose chemical instructions are followed
Define/explain: Trisomy 21 aka Down Syndrome
a genetic disorder that is caused by an extra 21st chromosome
Define: epigenesis
continuous interplay between genes and multiple levels of the environment (from cells to culture) that drives development
Define: gene
a group of nucleotide bases that provide a specific set of biochemical instructions
Define: genotype
the complete set of genes that makes up a person’s heredity
Define: monozygotic twins
identical twins, come from a single fertilized egg that split in two, have identical genes
Define: incomplete dominance
the situation in which one allele does not dominate another completely
Define/explain: in vitro fertilization
mixing sperm and egg together in a laboratory dish and then placing several fertilized eggs in a woman’s uterus
Define: heritability coefficient
the extent to which differences between people reflect heredity
Define: homozygous
a person who inherits the same allele on a pair of chromosomes, the biochemical instructions on the allele are followed
Define: Huntington’s disease
a type of dementia caused by a dominant allele; characterized by degeneration of the nervous system