Chapter 2 Heredity And Conception, Prenatal Development Flashcards
Heredity
Transmission of traits and characteristics from parent to child by genes
Genetics
The study of heredity
Chromosomes
Structures that are composed of genes and found within nuclei of cells, rod shaped
Gene
Basic unit of heredity composed of DNA
Polygenic
Resulting from many genes
Deoxyribonucleic Acid
Genetic material that takes the form of a double helix made up of phosphates, sugars, and bases
Zygote
An egg formed when the sperm and ovum join together
Mitosis
The form of cell division when chromosomes split lengthwise to double in number
Mutation
A sudden variation in a heritable characteristic affecting the composition of genes
Meiosis
The form of cell division in which each pair of chromosome splits and one member of each pair moves to the cell
Auto some
A member of a pair of chromosomes with the exception of sex chromosomes
Sex Chromosome
A chromosome that determines the sex of a child. X for a girl and Y for a boy.
Monozygotic Twins
Twins that derive from a single zygote that split into two identical twins
Dizygotic Twins
Twins that derive from two zygotes
Ovulation
The release of an ovum from an ovary
Allele
A member of a pair of genes
Homozygous
Having two identical alleles
Heterozygous
Having two different alleles
Dominant Trait
A trait that is expressed
Recessive Trait
A trait that is not expressed when the gene of genes involved have been paired with dominant genes. The traits are transmitted to future generations and expressed if paired with other recessive genes
Carrier
A person who carries and transmits characteristics but does not exhibit them
Multifactoral Problems
Problems that stem from heredity and environmental factors interacting
Down Syndrome
A chromosomal abnormality characterized by intellectual disability and caused by an extra 21st chromosome. Also known as Trisomy 21.
Sex-linked Chromosomal Abnormalities
Abnormalities that are transmitted from generation to generation, carried by a sex chromosome, usually an X sex chromosome.
Klinefelter Syndrome
A chromosomal disorder found among males that is caused by an X sex chromosome and is characterized by infertility and mild intellectual disability
Testosterone
A male sex hormone produced mainly by the testes
Turner Syndrome
A chromosomal disorder found among females that is caused by having a single X chromosome and characterized by infertility
Estrogen
A female sex hormone produced mainly by the ovaries
Phenylketonuria
A genetic abnormality in which phenylalanine builds up and causes intellectual disability
Huntington Disease
A fatal genetic neurological disorder whose onset is in middle age
Sickle-cell Anemia
A disorder decreasing the blood’s capacity to carry oxygen
Tay-Sachs Disease
A fatal disorder that destroys the nerve cells in the brain and spinal cord
Cystic Fibrosis
When mucus obstructs the lungs and pancreas
Hemophilia
When blood does not clot properly
Sex-linked abnormalities
Abnormalities resulting from genes found on the X sex chromosome.
Muscular Dystrophy
A chronic disease characterized by wasting away of the muscles
Genetic Counseling
Advice concerning the probabilities that a couple’s children will show genetic abnormalities
Prenatal
Before birth
Amniocentesis
A procedure for drawing out and examining fetal cells sloughed off into amniotic fluid to determine whether disorders are present
Spina Bifida
A neural tube defect that causes abnormalities of the brain and spine
Chorionic Villus Sampling
A method for the prenatal detection of genetic abnormalities that samples the membrane enveloping the amniotic sac and fluid
Uterus
The organ in females where the embryo and fetus develop
Ultrasound
Sound waves too high in pitch to be sensed by the human ear
Sonogram
A procedure for using ultrasonic sound waves to create a picture of an embryo and fetus
Alpha-Fetoprotein Assay
A blood test assesses the mother’s blood level of alpha feta protein, a substance linked to neural fetal tube defects
Reaction Range
The variability in the expression of inherited traits influenced by environmental factors
Genotype
The genetic form of a person as determined by heredity
Phenotype
The actual form of a person determined by heredity or environmental factors
Canalization
The tendency of growth rates to return to genetically determined patterns by undergoing environmentally induced change
Passive Genetic-Environmental Correlation
The correlation between the genetic endowment parents give their children and the environments in which they place their children
Evocative Genetic-Environmental Correlation
The correlation between the child’s endowment and the response the child elicits from other people
Active Genetic-environmental Correlational
The correlation between the child’s genetic endowment and the choices the child makes about which environment they will seek
Niche-Picking
Choosing environmental conditions that foster one’s genetically transmitted abilities and interests
Epigenesis
The view that development reflects continual bidirectional exchanges between genotypes and environmental conditions
Autism
A developmental disorder characterized by failure to relate to others, communication problems, intolerance of change, and ritualistic behavior
Conception
The union of a sperm cell and an ovum that occurs when the chromosome of each of these cells combine to form 23 pairs
Fallopian Tube
A tube through which ova travel from an ovary to the uterus
Endometrium
The inner lining of the uterus
Spontaneous Abortion
Accidental abortion, unplanned, also called miscarriage
Motility
Self-Propulsion
Pelvic Inflammatory Disease
An infection of the abdominal region that may have various causes and may impair fertility
Endometriosis
Inflammation of endometrial tissue sloughed off into the abdominal cavity rather than out of the body during menustration, the condition is characterized by abdominal pain and infertility
In Vitro Fertilization
Fertilization of an ovum or laboratory dish
Donor IVF
The transfer of a donor’s ovum fertilized in a laboratory dish to the uterus of another woman
Embryonic Transplant
The transfer of an embryo from the uterus of one woman to another
Surrogate Mother
A woman who is artificially inseminated and carries to term a child who is given to another woman, typically the spouse of a sperm donor
Artificial Insemination
Injection of sperm into the uterus to fertilize an ovum