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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.

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。

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引用本文的文献

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Delayed Diagnosis of a Pyloric Web Causing Gastric Outlet Obstruction in a 13-Month-Old Girl.一名13个月大女童因幽门蹼导致胃出口梗阻的延迟诊断
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Prenatally diagnosed congenital pyloric atresia in consecutive three siblings: a case report.连续三个兄弟姐妹产前诊断为先天性幽门闭锁:一例报告
Surg Case Rep. 2021 Jan 6;7(1):9. doi: 10.1186/s40792-020-01096-1.
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Congenital pyloric atresia: Early and delayed presentations-A single centre experience of a rare anomaly.
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Peculiar type 1 congenital pyloric atresia: a case report.特殊类型 1 型先天性幽门闭锁:1 例报告。
Ital J Pediatr. 2010 Jan 14;36:3. doi: 10.1186/1824-7288-36-3.