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Successful cardiac transplantation in Barth syndrome--single-centre experience of four patients.

Abstract
We describe four patients with Barth syndrome who have undergone successful orthotopic heart transplantation. Patients are one, seven, 12.5 and 14.7 yr post-transplantation. One episode of severe infection occurred. Renal dysfunction and coronary allograft vasculopathy do not appear accelerated over non-Barth patients. Despite withholding purine synthesis inhibitors, these patients have not demonstrated an increased rate of rejection.
AuthorsJasveer Mangat, Tracy Lunnon-Wood, Philip Rees, Martin Elliott, Michael Burch
JournalPediatric transplantation (Pediatr Transplant) Vol. 11 Issue 3 Pg. 327-31 (May 2007) ISSN: 1397-3142 [Print] Denmark
PMID17430492 (Publication Type: Case Reports, Journal Article)
Topics
  • Adolescent
  • Cardiomyopathies (etiology, surgery)
  • Child
  • Child, Preschool
  • Genetic Diseases, X-Linked (complications)
  • Heart Transplantation
  • Humans
  • Infant
  • Male
  • Metabolism, Inborn Errors (complications)
  • Syndrome
  • Treatment Outcome

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