与卵巢早衰有关的致病基因变异的发生率

S. Shekari, Stasa Stankovic, Eugene J. Gardner, G. Hawkes, K. Kentistou, R. Beaumont, A. Mörseburg, Andrew R. Wood, Julia K. Prague, Gita D. Mishra, F. Day, Julia Baptista, Caroline F. Wright, M. Weedon, Eva R. Hoffmann, K. Ruth, Ken K. Ong, John R. B. Perry, Anna Murray
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引用次数: 0

摘要

(摘自《自然医学》2023;29:1692-1699)早发性卵巢功能不全(Premature ovarian insufficiency,POI)是指在 40 岁之前发生的卵巢活动丧失和月经永久停止,影响 1%的女性,是导致不孕的主要原因之一。多达 90% 的卵巢功能不全病例是特发性的,其中多达 30% 的病例与家族遗传有关,这表明该病有遗传基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Penetrance of Pathogenic Genetic Variants Associated With Premature Ovarian Insufficiency
(Abstracted from Nat Med 2023;29:1692–1699) Premature ovarian insufficiency (POI), defined as the loss of ovarian activity and permanent cessation of menstruation occurring before age 40 years, affects 1% of women and is a leading cause of infertility. Up to 90% of POI cases are idiopathic, with up to 30% of those having some familial association, suggesting a genetic basis.
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