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nondisjunction |
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nondisjunction /non·dis·junc·tion/ (-dis-junk´shun) failure either of two homologous chromosomes to pass to separate cells during the first meiotic division, or of the two chromatids of a chromosome to pass to separate cells during mitosis or during the second meiotic division. As a result, one daughter cell has two chromosomes or two chromatids, and the other has none.
Nondisjunction A genetic term referring to an event which takes place during cell division, in which a genetic accident causes an egg or sperm cell to have 24 chromosomes, rather than the normal 23. Mentioned in: Down Syndrome
nondisjunction [-disjungk′chən] Etymology: L, non + disjungere, to disjoint failure of homologous pairs of chromosomes to separate during the first meiotic division or of the two chromatids of a chromosome to split during anaphase of mitosis or the second meiotic division. The result is an abnormal number of chromosomes in the daughter cells. Compare disjunction. See also monosomy, trisomy. nondisjunction [non″dis-jungk´shun] failure either of two homologous chromosomes to pass to separate cells during the first meiotic division, or of the two chromatids of a chromosome to pass to separate cells during mitosis or during the second meiotic division. As a result, one daughter cell has two chromosomes or two chromatids, and the other has none. If this happens during meiosis, an aneuploid individual (for example, a child with Down syndrome) may develop following fertilization. ![]() Nondisjunction. Normal meiosis (A) is contrasted with failure of homologous chromosomes to separate in meiosis I (B) or of sister chromatids to separate in meiosis II (C). From Dorland's, 2000. nondisjunction failure (1) of two homologous chromosomes to pass to separate cells during the first division of meiosis, or (2) of the two chromatids of a chromosome to pass to separate cells during mitosis or during the second meiotic division. As a result, one daughter cell has two chromosomes or two chromatids, and the other has none. Death of the fetus or chromosomal anomalies may result.
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