三倍体（69, XXX）的产前诊断（作者译）
[Prenatal diagnosis of triploidy (69, XXX) (author's transl)].
作者信息
Schlensker K H, Citoler P, Bolte A
出版信息
Geburtshilfe Frauenheilkd. 1979 Jul;39(7):588-92.
PMID:467953
Abstract
By amniocentesis we succeeded in finding a case of triploidy (69,XXX). Because of an extreme fetal dystrophy and missing fetal movements in the 33rd week a severe malformation was suspected. The clinical, ultrasonographical, cytogenetital, hormonal and autopsy findings are reported and discussed.
摘要
通过羊膜穿刺术，我们成功发现了一例三倍体（69,XXX）病例。由于孕33周时胎儿极度营养不良且胎动消失，怀疑存在严重畸形。现将临床、超声、细胞遗传学、激素及尸检结果报告并讨论如下。
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