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巨膀胱-小结肠-肠蠕动不良综合征的产前诊断

Prenatal diagnosis of the megacystis-microcolon-intestinal hypoperistalsis syndrome.

作者信息

Young I D, McKeever P A, Brown L A, Lang G D

机构信息

Department of Child Health, Leicester Royal Infirmary.

出版信息

J Med Genet. 1989 Jun;26(6):403-6. doi: 10.1136/jmg.26.6.403.

Abstract

The ultrasonographic and necropsy findings in a male fetus with the megacystis-microcolon-intestinal hypoperistalsis syndrome are reported. The presence of vacuolation and degeneration in smooth muscle of bowel and bladder wall supports a previous suggestion that the macroscopic findings in this syndrome are the consequence of an underlying visceral myopathy. The unusual degree of severity of the findings in this fetus may explain the marked skewing of the sex ratio observed in affected liveborn infants.

摘要

本文报告了一名患有巨膀胱-小结肠-肠蠕动不良综合征的男性胎儿的超声检查和尸检结果。肠壁和膀胱壁平滑肌出现空泡化和变性,这支持了之前的一种观点,即该综合征的宏观表现是潜在内脏肌病的结果。该胎儿中这些发现的异常严重程度可能解释了在受影响的活产婴儿中观察到的明显性别比例偏差。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df8d/1015629/598cf65b6f90/jmedgene00056-0052-a.jpg

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