作者
Osama A Bawazir, Ahmed H Al-Salem
发表日期
2017/10/1
期刊
Annals of Pediatric Surgery
卷号
13
期号
4
页码范围
188-193
出版商
LWW
简介
Background
Congenital pyloric atresia (CPA) is very rare and usually seen as an isolated anomaly, which has an excellent prognosis. CPA can be associated with other anomalies or familial and these are usually associated with other hereditary conditions with poor prognosis. This review is based on our experience with 20 infants with CPA.
引用总数
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