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家族性15-22易位。女性携带者流产的一个可能原因。

Familial translocation 15-22. A possible cause for abortions in female carriers.

作者信息

Fried K, Bukovsky J, Rosenblatt M, Mundel G

出版信息

J Med Genet. 1974 Sep;11(3):280-2. doi: 10.1136/jmg.11.3.280.

Abstract

A familial Robertsonian translocation 15/22 was ascertained through a female carrier whose four pregnancies ended in missed abortions. Eleven 15/22 translocation carriers were detected in three generations among 23 family members investigated. The four proven female carriers, apart from the proposita, have miscarried seven out of 14 pregnancies. The kindred suggests that the 15/22 translocation in female carriers may cause an increased risk for miscarriage.

摘要

通过一名女性携带者确诊了15/22罗伯逊易位,该携带者的四次怀孕均以稽留流产告终。在调查的23名家庭成员中的三代人中检测到11名15/22易位携带者。除先证者外,4名已证实的女性携带者在14次怀孕中有7次流产。该家族表明女性携带者中的15/22易位可能会增加流产风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a600/1013143/f47c207357af/jmedgene00320-0061-a.jpg

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