1) Congenital esophageal atresia
先天性食管闭锁
1.
Respiratory management of perioperative patients with congenital esophageal atresia accompanied by tracheo-esophageal fistula;
先天性食管闭锁伴气管食管瘘围术期的呼吸管理
2.
Intensive care of neonates with type III congenital esophageal atresia;
Ⅲ型先天性食管闭锁新生儿的术后监护
2) congenital atresia of esophagus
先天性食管闭锁
1.
Nursing of ill neonates with Ⅲ-type congenital 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
补充资料：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。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条