先天性肥厚性幽门狭窄的诊治进展
摘要
先天性肥厚性幽门狭窄（Congenital Hypertrophic Pyloric Stenosis，CHPS）是新生儿常见的消化道畸形，发病率在国外较高，达1．5‰～4．0‰，国内稍低，为0．3‰～1．0‰，均为足月婴幼儿，头胎多见，男性占80％，男女发病率比冽约为4～8：1^[1]。CHPS是由于新生儿幽门肌层（尤其是环形肌）过度增生、肥厚导致幽门管狭窄的上消化道梗阻性疾病，症状多于出生2周后出现，
出处
《中国消化内镜》
2008年第4期33-36,共4页
Digestive Disease and Endoscopy
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共引文献14
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