患有眼部异常和小头畸形的同胞中的苹果皮样肠闭锁。

Apple peel intestinal atresia in siblings with ocular anomalies and microcephaly.

作者信息

Strømme P, Dahl E, Flage T, Stene-Johansen H

机构信息

Department of Paediatrics, Rikshospitalet, Oslo, Norway.

出版信息

Clin Genet. 1993 Oct;44(4):208-10. doi: 10.1111/j.1399-0004.1993.tb03881.x.

DOI:10.1111/j.1399-0004.1993.tb03881.x

PMID:8261651

Abstract

Two siblings who presented shortly after birth with signs of upper intestinal obstruction were successfully operated for apple peel jejunal atresia. In addition to intestinal malformations, both siblings exhibited severe microcephaly and ocular abnormalities not previously reported in this condition.

摘要

两名出生后不久即出现上消化道梗阻症状的兄弟姐妹成功接受了苹果皮样空肠闭锁手术。除肠道畸形外，这两名兄弟姐妹均表现出严重小头畸形和眼部异常，此前这种情况未曾有过报道。