新生儿先天性巨结肠诊断与治疗研究进展

先天性巨结肠（HD）又称肠无神经节细胞症,是引起新生儿消化道梗阻的常见原因,是小儿外科常见而较严重的先天性消化道畸形,发病率为0.02%~0.05%,男女比例为4∶1[1],且有一定的遗传易感性。近10余年,HD诊断、治疗均有显著进展,以至新生儿及婴儿可获得明确诊断及行根治手术。本文就新生儿HD诊治的各种方法的现状及最新研究进展综述如下。...

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Published in现代医药卫生 Vol. 31; no. 13; pp. 1966 - 1969
Main Author 李洪 金先庆
Format Journal Article
LanguageChinese
Published 重庆医科大学附属儿童医院胃肠新生儿外科,重庆,400014 2015
Subjects
Hirschsprung病/治疗
Hirschsprung病/诊断
婴儿,新生,疾病
综述
Hirschsprung病/治疗
综述
Hirschsprung病/诊断
婴儿,新生,疾病
Online AccessGet full text
ISSN1009-5519
DOI10.3969/j.issn.1009-5519.2015.13.014

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Abstract 先天性巨结肠（HD）又称肠无神经节细胞症,是引起新生儿消化道梗阻的常见原因,是小儿外科常见而较严重的先天性消化道畸形,发病率为0.02%~0.05%,男女比例为4∶1[1],且有一定的遗传易感性。近10余年,HD诊断、治疗均有显著进展,以至新生儿及婴儿可获得明确诊断及行根治手术。本文就新生儿HD诊治的各种方法的现状及最新研究进展综述如下。
AbstractList 先天性巨结肠（HD）又称肠无神经节细胞症,是引起新生儿消化道梗阻的常见原因,是小儿外科常见而较严重的先天性消化道畸形,发病率为0.02%~0.05%,男女比例为4∶1[1],且有一定的遗传易感性。近10余年,HD诊断、治疗均有显著进展,以至新生儿及婴儿可获得明确诊断及行根治手术。本文就新生儿HD诊治的各种方法的现状及最新研究进展综述如下。
Author 李洪 金先庆
AuthorAffiliation 重庆医科大学附属儿童医院胃肠新生儿外科,重庆400014
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综述
Hirschsprung病/诊断
婴儿,新生,疾病
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Snippet 先天性巨结肠（HD）又称肠无神经节细胞症,是引起新生儿消化道梗阻的常见原因,是小儿外科常见而较严重的先天性消化道畸形,发病率为0.02%~0.05%,男女比例为4∶1[1],且有一定...
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StartPage 1966
SubjectTerms Hirschsprung病/治疗
Hirschsprung病/诊断
婴儿,新生,疾病
综述
Title 新生儿先天性巨结肠诊断与治疗研究进展
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