1. MUTATIONS B-4.8

2. MUTATIONS A mutation is the alteration of an organism’s DNA. Mutations can result from a malfunction during the process of meiosis or exposure to a physical or chemical agent called a mutagen. Most mutations are automatically repaired by the organism’s enzymes and therefore have no effect. However, when a mutation is not repaired, it results in a mutant cell.

3. MUTATIONS If the mutant cell is a sex cell or gamete, it can result in a genetic disorder. If the mutation affects a single gene, it is known as a gene mutation. Examples of genetic disorders: a. Sickle-cell disease is a mutation that affects the hemoglobin in blood and is found predominantly in African-Americans. b. Other examples are Tay-Sachs disease, Huntington’s disease, cystic fibrosis, or albinism.

4. MUTATIONS If the mutation affects a group of genes or an entire organism, it is known as a chromosomal mutation. Nondisjunction results in an abnormal number of chromosomes, usually occurring during meiosis.  Examples of abnormalities in humans due to nondisjunction of sex chromosomes are Klinefelter’s syndrome (male) and Turner’s syndrome (female).  Examples of abnormalities in humans due to nondisjunction of autosomal chromosomes include Down syndrome.