Intrahepatic cholestasis of pregnancy: When should you look further?

Open Access
Authors
  • W. Hardikar
  • S. Kansal
  • R.P.J. Oude Elferink
  • P. Angus
Publication date 2009
Journal World Journal of Gastroenterology
Volume | Issue number 15 | 9
Pages (from-to) 1126-1129
Organisations
  • Faculty of Medicine (AMC-UvA)
Abstract
Pruritis with abnormal liver function tests is the classical presentation of intrahepatic cholestasis of pregnancy (ICP), a condition associated with significant fetal complications. Although the etiology of ICP is unclear in many cases, certain features of the clinical presentation should alert the practitioner to the possibility of an underlying metabolic defect, which may not only affect subsequent pregnancies, but may be an indicator of more serious subsequent liver disease. We report a kindred of Anglo-Celtic descent, among whom many members present with ICP, gallstones or cholestasis related to use of oral contraception. Genetic studies revealed a novel mutation in the ABCB4 gene, which codes for a phospholipid transport protein. The clinical significance of this mutation and the importance of identifying such patients are discussed. (C) 2009 The WIG Press and Baishideng. All rights reserved
Document type Article
Published at https://doi.org/10.3748/wjg.15.1126
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