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- W2139372472 endingPage "553" @default.
- W2139372472 startingPage "541" @default.
- W2139372472 abstract "Progressive familial intrahepatic cholestasis (PFIC) type 1, 2 and 3 are due to mutations in ATP8B1, ABCB11 and ABCB4, respectively. Each of these genes encodes a hepatocanalicular transporter, which is essential for the proper formation of bile. Mutations in ABCB4 can result in progressive cholestatic disease, while mutations in ATP8B1 and ABCB11 can result both in episodic cholestasis, referred to as benign recurrent intrahepatic cholestasis (BRIC) type 1 and 2, as well as in progressive cholestatic disease. This suggests a clinical continuum and these diseases are therefore preferably referred to as ATP8B1 deficiency and ABCB11 deficiency. Similarly PFIC type 3 is designated as ABCB4 deficiency. Heterozygous mutations in each of these transporters can also be associated with intrahepatic cholestasis of pregnancy. This review summarizes the pathophysiology, clinical features and current as well as future therapeutic options for progressive familial- and benign recurrent intrahepatic cholestasis as well as intrahepatic cholestasis of pregnancy." @default.
- W2139372472 created "2016-06-24" @default.
- W2139372472 creator A5001393272 @default.
- W2139372472 creator A5006966232 @default.
- W2139372472 creator A5020425160 @default.
- W2139372472 creator A5034630836 @default.
- W2139372472 creator A5055247870 @default.
- W2139372472 creator A5058559696 @default.
- W2139372472 date "2010-10-01" @default.
- W2139372472 modified "2023-10-02" @default.
- W2139372472 title "Familial cholestasis: Progressive familial intrahepatic cholestasis, benign recurrent intrahepatic cholestasis and intrahepatic cholestasis of pregnancy" @default.
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