Document Detail

Alagille syndrome and other hereditary causes of cholestasis.
MedLine Citation:
PMID:  23540503     Owner:  NLM     Status:  MEDLINE    
Neonatal conjugated jaundice is a common presentation of hereditary liver diseases, which, although rare, are important to recognize early. Developments in molecular genetic techniques have enabled the identification of causative genes, which has improved diagnostic accuracy for patients and has led to a greater understanding of the molecular pathways involved in liver biology and pathogenesis of liver diseases. This review provides an update of the current understanding of clinical and molecular features of the inherited liver diseases that cause neonatal conjugated jaundice.
Jane L Hartley; Paul Gissen; Deirdre A Kelly
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Publication Detail:
Type:  Journal Article; Review    
Journal Detail:
Title:  Clinics in liver disease     Volume:  17     ISSN:  1557-8224     ISO Abbreviation:  Clin Liver Dis     Publication Date:  2013 May 
Date Detail:
Created Date:  2013-04-01     Completed Date:  2013-11-15     Revised Date:  2014-02-24    
Medline Journal Info:
Nlm Unique ID:  9710002     Medline TA:  Clin Liver Dis     Country:  United States    
Other Details:
Languages:  eng     Pagination:  279-300     Citation Subset:  IM    
Copyright Information:
Copyright © 2013 Elsevier Inc. All rights reserved.
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MeSH Terms
Alagille Syndrome / complications*,  diagnosis,  drug therapy,  genetics
Cholestasis / etiology*,  genetics
Grant Support
095662//Wellcome Trust

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