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进行性家族性肝内胆汁淤积症3型:2例报道并文献复习
Type 3 progressive familial intrahepatic cholestasis: 2 cases report and literature review
【摘要】 进行性家族性肝内胆汁淤积症是一组罕见的常染色体隐性遗传病,起病早,进展快,死亡率高,治疗较为困难。本文报道进行性家族性肝内胆汁淤积症3型2例,并附文献复习。
【Abstract】 Progressive familial intrahepatic cholestasis is a group of rare autosomal recessive genetic disease with early onset,rapid progression,high mortality and difficult treatment. This paper reported 2 cases of type 3 progressive familial intrahepatic cholestasis and literature review.
【关键词】 进行性家族性肝内胆汁淤积症;
遗传病;
儿童;
【Key words】 Progressive familial intrahepatic cholestasis; Genetic disease; Children;
【Key words】 Progressive familial intrahepatic cholestasis; Genetic disease; Children;
【基金】 郑加生专家工作站(2018IC115)
- 【文献出处】 胃肠病学和肝病学杂志 ,Chinese Journal of Gastroenterology and Hepatology , 编辑部邮箱 ,2020年02期
- 【分类号】R575
- 【被引频次】2
- 【下载频次】186