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<正>先天性肛门闭锁是在胚胎第4～8周时由尿生殖隔向泄殖腔移行受阻所致,是常见的消化道畸形,占消化道畸形的首位,发生率约为1/1 500～1/5000[1],男多于女,男女比例约为3:1,无种族差异,部分病例有家性发病族倾向[2];据国内畸形监测网统计,在我国的发生率是2.81/万。随着现代影像学逐步应用于临床和现代微创技术在小儿外科应
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基本信息:
DOI：10.13210/j.cnki.jhmu.2013.06.023
中图分类号:R726.5
引用信息:
[1]龙雪峰,李强辉.先天性肛门闭锁的诊治进展[J].海南医学院学报,2013,19(06):861-864.DOI:10.13210/j.cnki.jhmu.2013.06.023.
基金信息:
中国高校医学期刊临床专项资金项目(112210690)
2013-03-27
2013-03-27
2013-03-27