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Resolution of xanthomas in Alagille syndrome after liver transplantation.

Abstract
Alagille syndrome (arteriohepatic dysplasia) is a genetic disorder with autosomal dominant transmission which has been localized to chromosome 20p. Cutaneous manifestations include jaundice, pruritus, and widespread xanthomata. We report a child with severe Alagille syndrome in whom orthotopic liver transplantation caused rapid resolution of disfiguring xanthomas.
AuthorsD A Buckley, E M Higgins, A W du Vivier
JournalPediatric dermatology (Pediatr Dermatol) 1998 May-Jun Vol. 15 Issue 3 Pg. 199-202 ISSN: 0736-8046 [Print] United States
PMID9655315 (Publication Type: Case Reports, Journal Article)
Topics
  • Alagille Syndrome (complications, surgery)
  • Child
  • Follow-Up Studies
  • Hand Dermatoses (etiology, physiopathology)
  • Humans
  • Liver Transplantation (adverse effects)
  • Male
  • Xanthomatosis (etiology, physiopathology)

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