High urgency liver transplantation in ornithine transcarbamylase deficiency presenting with acute liver failure

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Ulrike Teufel - , Heidelberg University  (Author)
  • Jürgen Weitz - , Heidelberg University  (Author)
  • Christa Flechtenmacher - , Heidelberg University  (Author)
  • Viola Prietsch - , Städtischen Klinikum Karlsruhe (Author)
  • Jan Schmidt - , Heidelberg University  (Author)
  • Georg F. Hoffmann - , Heidelberg University  (Author)
  • Stefan Kölker - , Heidelberg University  (Author)
  • Guido Engelmann - , Heidelberg University  (Author)

Abstract

OTCD can present with ALF at any age. Under adequate therapy symptoms resolve quickly. We report a three-yr-old girl with the manifestation of an OTCD as ALF. Despite adequate pharmacotherapy and protein restriction, the patient deteriorated and developed hepatic encephalopathy. A high urgency liver transplantation was performed and the patient recovered completely. We conclude that in patients with ALF urea cycle defects in general and OTCD in particular should be considered as differential diagnosis. Patients should be managed in a center that has the capacity for an emergency liver transplantation.

Details

Original languageEnglish
Pages (from-to)E110-E115
JournalPediatric transplantation : the official publication of the International Pediatric Transplant Association
Volume15
Issue number6
Publication statusPublished - Sept 2011
Peer-reviewedYes
Externally publishedYes

External IDs

PubMed 21884343

Keywords

Keywords

  • acute liver failure, metabolic, pediatric liver transplantation, urea cycle disorder