先天性肠闭锁(congenital intestinal atresia)是指 胚胎期肠管发育在再管化过程中部分肠道终止发育造成肠腔完全或部分阻塞。完全阻塞为闭锁，部分阻塞则为狭窄。
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Method: The clinical data of 45 cases of congenital intestinal atresia in our hospital between 1996 to 2008 was reviewed.
方法：总结分析我院1996年至2008年45例先天性肠闭锁的临床资料。
Objective To evaluate the distribution of ganglia cells in congenital intestinal atresia and discuss the clinical significance.
目的了解神经节细胞在先天性小肠闭锁中的分布情况，并探讨其临床意义。
Methods The clinic data of 40 cases of congenital intestinal atresia were reviewed, including duodenal atresia8, jejunal atresia8 and ileum atresia24.
方法对40例先天性肠闭锁的患儿进行回顾性分析，其中十二指肠闭锁8例，空肠闭锁8例，回肠闭锁24例；
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