DEV CHAPTER 2 | HEREDITY, PRENATAL DEVELOPMENT, AND BIRTH Flashcards
specific sequence of nucleotides and are recipes for making proteins
Genes
the cell’s nucleus making an exact copy of all the chromosomes and splitting into two new cells.
Mitosis
the gamete’s chromosomes duplicate, and then divide twice resulting in four cells containing only half the genetic material of the original gamete
meiosis
refers to the sum total of all the genes a person inherits
genotype
refers to the features that are actually expressed.
phenotype
we may receive either the same version of a gene from our mother and father
homozygous
If we receive a different version of the gene from each parent
heterozygous
express themselves in the phenotype even when paired with a different version of the gene
dominant genes
express themselves only when paired with a similar version gene
recessive genes
geneticists refer to different versions of a gene
alleles
meaning they are the result of several genes
polygenic
sometimes the dominant gene does not completely suppress the recessive gene
incomplete dominance
occur when a fertilized egg splits apart in the first two weeks of development
Monozygotic or identical twins
those who have inherited only one recessive-gene
carriers
two eggs or ova are released and fertilized by two separate sperm
dizygotic or fraternal twins
the defective gene is found on the X-chromosome
sex-linked
The individual inherits a gene change from both parents. If the gene is inherited from just one parent, the person is a carrier and does not have the condition.
Recessive Disorders (Homozygous):
a condition in which the red blood cells in the body are shaped like a sickle (like the letter C) and affect the ability of the blood to transport oxygen.
Sickle Cell Disease (SCD)
a condition that affects breathing and digestion due to thick mucus building up in the body, especially the lungs and digestive system.
Cystic Fibrosis (CF)
a tic disorder which results in uncontrollable motor and vocal tics as well as body jerking.
Tourette Syndrome
a metabolic disorder in which the individual cannot metabolize phenylalanine, an amino acid.
Phenylketonuria (PKU)
caused by enzyme deficiency resulting in the accumulation of lipids in the nerve cells of the brain
Tay Sachs Disease
when the individual lacks melanin and possesses little to no pigment in the skin, hair, and eyes.
Albinism
In order to have the disorder, the individual only needs to inherit the gene change from one parent
Autosomal Dominant Disorders (Heterozygous):