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.
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Authors | Jasveer Mangat, Tracy Lunnon-Wood, Philip Rees, Martin Elliott, Michael Burch |
Journal | Pediatric transplantation
(Pediatr Transplant)
Vol. 11
Issue 3
Pg. 327-31
(May 2007)
ISSN: 1397-3142 [Print] Denmark |
PMID | 17430492
(Publication Type: Case Reports, Journal Article)
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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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