罕见的胎儿腹裂合并足部及外生殖器发育不全病例。

Rare case of fetal gastroschisis with aplasia of the foot and external genital organs.

作者信息

Rao Suresh Rangoji, Rao T Ramesh, Gajula Somu Sekhar, Rao A V C

机构信息

Department of Preclinical Sciences, Faculty of Medical Sciences, The University of the West indies, St Augustine, Trinidad and Tobago, West Indies.

出版信息

Congenit Anom (Kyoto). 2008 Sep;48(3):140-1. doi: 10.1111/j.1741-4520.2008.00194.x.

DOI:10.1111/j.1741-4520.2008.00194.x

PMID:18778459

Abstract

Gastroschisis is a rare anomaly and is usually not associated with any other congenital anomalies. The embryology of gastroschisis and omphalocele remains a matter of speculation. Incidences of gastroschisis are particularly high among pregnancies in very young women. The present case is reported because of its rare association with the condition of gastroschisis, disrupted omphalocele, with aplasia of the foot and external genital organs, as well as imperforate anus with distal rectal atresia.

摘要

腹裂是一种罕见的异常情况，通常不伴有任何其他先天性异常。腹裂和脐膨出的胚胎学仍然是一个推测的问题。腹裂在非常年轻女性的妊娠中发生率特别高。本病例之所以被报道，是因为它罕见地合并了腹裂、破裂的脐膨出、足部和外生殖器发育不全，以及肛门闭锁伴远端直肠闭锁的情况。