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Anatomy · Medical genetics: origin of nondisjunction
Sample itemIn most cases of trisomy 21 with a standard 47,XX,+21 karyotype, in which parent and at which stage did the error occur?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
B. Maternal meiosis I
About nine in ten cases of standard trisomy 21 arise from nondisjunction in the mother, most often at meiosis I. The risk rises with maternal age because oocytes remain arrested in prophase I for decades.
Option by option
A. Maternal meiosis II
Maternal meiosis II errors occur but are less common than meiosis I errors.
B. Maternal meiosis I (correct)
Correct. Most extra chromosomes 21 come from the mother, usually from a meiosis I error.
C. Paternal meiosis I
Paternal errors account for a small minority of cases.
D. Post-zygotic mitosis
Post-zygotic mitotic errors produce mosaicism rather than the standard full trisomy.
Source note: Original NextPrep sample item — pending expert review. This item is original practice material awaiting independent expert review, so confirm important facts in a standard textbook.
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