| Literature DB >> 21108711 |
David Buchbinder1, Diane Nugent, Dan Vu, Amit Soni, Jill Stites, Loan Hsieh, Geetha Puthenveetil.
Abstract
CDA is a heterogeneous group of disorders that result in morphologically abnormal erythroid maturation and ineffective erythropoiesis. Curative therapy for CDA focuses on the use of HSCT using fully matched sibling donors. This is the first report of a Type II CDA patient with severe iron overload who was successfully treated with HSCT using a HLA-matched unrelated donor after aggressive chelation therapy. Given the challenges of HSCT in any patient with CDA and severe iron overload, the role of novel approaches to iron chelation and HSCT is discussed.Entities:
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Year: 2010 PMID: 21108711 DOI: 10.1111/j.1399-3046.2010.01414.x
Source DB: PubMed Journal: Pediatr Transplant ISSN: 1397-3142