泄殖腔膜发育不全。可能的致畸异常。

Perspectives in pediatric pathology Pub Date : 1984-01-01
H B Robinson, K Tross
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引用次数: 0

摘要

在7个半月的时间里,我们在一个社区里遇到了5名患有罕见而独特的畸形复合物的婴儿。在1926年至1980年的54年间,只有7份关于这种情况的报告被发现。在先前发表的病例中,主要发现是没有外生殖器、尿道、生殖器和肛门口,以及持续的泄殖腔。本报告记录了该综合征在时间和区域集群中的发生。对每个婴儿的详细形态学评估为该复合体的胚胎发生理论提供了基础,初步数据表明是致畸原因。3例妊娠前50天胚胎暴露于琥珀酸多西胺是确定的,5例妊娠中有2例是可能的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Agenesis of the cloacal membrane. A probable teratogenic anomaly.

Five infants with a rare and distinct malformation complex were encountered in a single community within a 7 1/2-month period. Only seven previous reports of this condition were found in the 54-year period between 1926 and 1980. The principal findings in the previously published cases were absence of external genitalia, urinary, genital, and anal orifices, and persistence of the cloaca. This report documents the occurrence of the syndrome in a temporal and regional cluster. Detailed morphologic evaluation of each infant provides the basis for a theory of embryogenesis of the complex, and preliminary data suggest a teratogenic cause. Embryonic exposure to doxylamine succinate within the first 50 days of the pregnancy was certain in three and was probable in two of the five pregnancies.

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