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Nondisjunction Disorders
- mistakes during meiosis
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If sister chromatids do not separate during meiosis I or II, an egg or a sperm may end up with too many chromosomes of one type (3 instead of 2)
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The extra copies of chromosomes result in abnormal embryonic development, ex. Down syndrome (trisomy 21) Round, full face Impaired intelligence Hand, tongue, eyelid abnormalities Short height Cardiac abnormalities
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Trisomies are very common in human zygotes: 10-30% of all conceptions
Most trisomies (other than for chromosome 21) are lethal to the embryo: at least one-fifth of all recognized pregnancies spontaneously terminate (miscarry) during the first two months of pregnancy 1 in 600 babies are born with Down syndrome
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Statistics for Down Syndrome
The risk of having a baby with Down syndrome increases with the mother’s age
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Other nondisjunction disorders:
1. Turner syndrome Monosomic: a female with a single X chromosome Individual appears female but does not develop secondary sexual characteristics Short, have thick, widened necks 1 in 3000 female babies
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2. Klinefelter syndrome Nondisjunction in either the sperm or egg, the child inherits two X chromosomes and a single Y chromosome Child appears male at birth, but develops female secondary sexual characteristics
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