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两例同胞先天性肝外胆管闭锁(作者译)

[Congenital atresia of the extrahepatic bile-ducts in two siblings (author's transl)].

作者信息

Schulte M J, Lenz W

出版信息

Klin Padiatr. 1978 Sep;190(5):512-8.

PMID:568202
Abstract

Congenital atresia of the extrahepatic bile-ducts in two siblings (boy and girl) with parental consanguinity is reported. Diagnosis is based on liver biopsy. In one case (boy) laparotomy was performed. An attempt at reconstructive surgery of the biliary tract was unsuccessful and the boy died at the age of 13 months. Only a small number of cases with familiar congenital extrahepatic biliary atresia have been published to date.

摘要

报告了一对有近亲关系的同胞(男孩和女孩)患有先天性肝外胆管闭锁的病例。诊断基于肝脏活检。其中一例(男孩)进行了剖腹手术。胆道重建手术尝试未成功,该男孩于13个月大时死亡。迄今为止,仅有少数家族性先天性肝外胆管闭锁的病例被发表。

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