Cholestatic syndromes

被引:10
作者
Trauner, M [1 ]
Boyer, JL [1 ]
机构
[1] Yale Univ, Yale Liver Ctr, Sch Med, New Haven, CT 06520 USA
关键词
D O I
10.1097/00001574-200205000-00005
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Further insights into the molecular regulation of bile acid transport and metabolism have provided the basis for a better understanding of the pathogenesis of cholestatic liver diseases. Novel insights into the mechanisms of action of ursodeoxycholic acid should advance our understanding of the treatment of cholestatic liver diseases. Mutations of transporter genes can cause hereditary cholestatic syndromes in both infants and adults as well as cholesterol gallstone disease. Important studies have been published on the pathogenesis, clinical features, and treatment of primary biliary cirrhosis, drug-induced cholestasis, and cholestasis of pregnancy. (C) 2002 Lippincott Williams Wilkins, Inc.
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收藏
页码:314 / 329
页数:16
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