家族性先天性幽门闭锁的产前诊断
Prenatal diagnosis of familial congenital pyloric atresia.
作者信息
Peled Y, Hod M, Friedman S, Mashiach R, Greenberg N, Ovadia J
机构信息
Department of Obstetrics and Gynecology, Beilinson Medical Center, Petah Tiqva, Israel.
出版信息
Prenat Diagn. 1992 Feb;12(2):151-4. doi: 10.1002/pd.1970120212.
PMID:1553362
Abstract
Familial congenital pyloric atresia is a rare malformation of the fetal gastrointestinal tract. It usually manifests as maternal polyhydramnios and enlarged fetal stomach on ultrasound scan. Sonographic prenatal diagnosis and management of a pregnancy complicated by familial congenital pyloric atresia are presented.
摘要
家族性先天性幽门闭锁是一种罕见的胎儿胃肠道畸形。它通常表现为母亲羊水过多，超声扫描显示胎儿胃部增大。本文介绍了一例合并家族性先天性幽门闭锁妊娠的超声产前诊断及处理。
Zotero 插件