先天性十二指肠闭锁(congenital duodenal atresia) 是胚胎时期，肠管空泡化不全所引致，属肠管发育障碍性疾病。病儿可伴有其他发育畸形，如21号染色体三体畸形（先天愚型，Down
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Surgical operation confirmed that 46 cases with malrotation of intestines, 24 with congenital duodenal atresia or stenosis (including membranous stenosis) and 15 with annular pancreas.
手术证实肠旋转不良46例；先天性十二指肠狭窄或闭锁(包括膜式闭锁)24例，环状胰腺15例。
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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