先天性食管闭锁,Congenital esophageal atresia
congenital atresia of esophagus先天性食管闭锁
1.Nursing of ill neonates with Ⅲ-typecongenital atresia of esophagus during operation;Ⅲ型先天性食管闭锁患儿的术中护理
3)biliary atresia(BA)先天性胆管闭锁
1.Objective To evaluate the value of biochemical markers in the diagnosis of biliary atresia(BA) and neonatal intrahepatic cholestasis caused by citrin deficiency(NICCD).目的新生儿肝内胆汁淤积综合征(NICCD)和先天性胆管闭锁(BA)是婴儿肝炎综合征的2个常见原因。
4)ia of esophagus后天性食管闭锁
5)congenital atresia of vas deferens先天性输精管闭锁
6)resia of ejaculatory duct先天性射精管闭锁
延伸阅读
食管闭锁食管闭锁esophageal atresia是一种先天性食管畸形。原因是胚胎发育至第3~6周之间,出现发育异常,造成食管隔断,成盲端或与气管、支气管相通形成食管-支气管瘘。症状为患儿吮吸奶汁立即呕吐或出现严重呛咳、发绀或窒息。通过食管放置导管并注入碘油行X线检查可确诊。治疗原则为首先挽救患者生命,再重建消化道连续性,尽可能利用食管。