Two Cases of Progressive Familial Intrahepatic Cholestasis Type 2 Presenting with Severe Coagulopathy without Jaundice
Joint Authors
Hertel, Paula
Karwowski, Christine
Tibesar, Eric
Scheimann, Ann
Karnsakul, Wikrom
Source
Issue
Vol. 2014, Issue 2014 (31 Dec. 2014), pp.1-4, 4 p.
Publisher
Hindawi Publishing Corporation
Publication Date
2014-06-02
Country of Publication
Egypt
No. of Pages
4
Main Subjects
Abstract EN
Progressive familial intrahepatic cholestasis (PFIC) type 2 results from a mutation in the bile salt exporter pump, impeding bile acid transport.
Patients usually present with jaundice, pruritus, growth failure, and fat soluble vitamin deficiencies.
We present two patients diagnosed with PFIC type 2 due to severe coagulopathy and bleeding without jaundice.
American Psychological Association (APA)
Tibesar, Eric& Karwowski, Christine& Hertel, Paula& Scheimann, Ann& Karnsakul, Wikrom. 2014. Two Cases of Progressive Familial Intrahepatic Cholestasis Type 2 Presenting with Severe Coagulopathy without Jaundice. Case Reports in Pediatrics،Vol. 2014, no. 2014, pp.1-4.
https://search.emarefa.net/detail/BIM-452831
Modern Language Association (MLA)
Tibesar, Eric…[et al.]. Two Cases of Progressive Familial Intrahepatic Cholestasis Type 2 Presenting with Severe Coagulopathy without Jaundice. Case Reports in Pediatrics No. 2014 (2014), pp.1-4.
https://search.emarefa.net/detail/BIM-452831
American Medical Association (AMA)
Tibesar, Eric& Karwowski, Christine& Hertel, Paula& Scheimann, Ann& Karnsakul, Wikrom. Two Cases of Progressive Familial Intrahepatic Cholestasis Type 2 Presenting with Severe Coagulopathy without Jaundice. Case Reports in Pediatrics. 2014. Vol. 2014, no. 2014, pp.1-4.
https://search.emarefa.net/detail/BIM-452831
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references
Record ID
BIM-452831
