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CN 22-1108/R
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Jan.  2018
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Article Navigation >  Journal of Clinical Hepatology  > 2018  >  34(1): 179-180

A case report of benign recurrent intrahepatic cholestasis

DOI: 10.3969/j.issn.1001-5256.2018.01.038

  • Department of Hepatology, The Fifth People′s Hospital of Suzhou, Suzhou, Jiangsu 215007, China

  • Published Date: 2018-01-20
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    • References(5)
  • [1]EIBERG H, NØRGAARD-PEDERSEN B, NIELSEN IM.Cholestasis Familiaris Groenlandica/Byler-like disease in Greenland——a population study[J].Int J Circumpolar Health, 2004, 63 (Suppl 2) :189-191.
    [2]KLOMP LM, BULL LN, KINSLEY AS, et al.A missense mutation in FIC1 is associated with greenland familial cholestasis[J].Hepatology, 2000, 32 (6) :1337-1341.
    [3]NICOLAS I, PONS JA, VARGAS A, et al.Ursodeoxycholic acid treatment shortens the course of cholestasis in two patients with benign recurrent intrahepatic cholestasis[J].Gastroenterol Hepatol, 2003, 26 (7) :421-423.
    [4]STAPELBROEK JM, van ERPECUM KJ, KLOMP LW, et al.Nasobiliary drainage induces long-lasting remission in benign recurrent intrahepatic cholestasis[J].Hepatology, 2006, 43 (1) :51-53.
    [5]van OOTEGHEM NA, KLOMP LW, van BERGE-HENEGOUWEN GP, et al.Benign recurrent intrahepatic cholestasis progressing to progressive familial intrahepatic cholestasis:low GGT cholestasis is a clinical continuum[J].J Hepatol, 2002, 369 (3) :439-443.
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