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21三体综合征及X/XX性染色体嵌合体的产前诊断

Prenatal diagnosis of trisomy 21 and X/XX sex chromosome mosaicism.

作者信息

McCorquodale M M, Cummins T, Furlong J

出版信息

Prenat Diagn. 1985 Jul-Aug;5(4):295-8. doi: 10.1002/pd.1970050409.

Abstract

Double aneuploidy involving Down syndrome and Turner syndrome is a rare chromosomal abnormality presumed to occur with a frequency of about 1 in 2 million births. Twenty-one cases of this combined anomaly have been reported and two infants were born with this anomaly after a mistake in prenatal diagnosis. We report the first prenatal diagnosis of Down syndrome combined with Turner mosaicism and suggest that this polysyndrome may be more common than previously estimated. We, therefore, wish to alert cytogenetic laboratories performing prenatal diagnoses of the potential risks of misdiagnosis of this polysyndrome if banding is not performed and if a sufficient number of mitotic cells are not analysed.

摘要

涉及唐氏综合征和特纳综合征的双非整倍体是一种罕见的染色体异常,据推测其发生频率约为每200万例出生中出现1例。已有21例这种联合异常的病例报告,并且有两名婴儿在产前诊断失误后出生时患有这种异常。我们报告了首例唐氏综合征合并特纳嵌合体的产前诊断,并表明这种多综合征可能比之前估计的更为常见。因此,我们希望提醒进行产前诊断的细胞遗传学实验室,如果不进行显带分析且未分析足够数量的有丝分裂细胞,就存在误诊这种多综合征的潜在风险。

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