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J Pediatr Hematol Oncol ; 35(7): 570-2, 2013 Oct.
Article in English | MEDLINE | ID: mdl-23337553

ABSTRACT

A now 10-year-old Laotian female was delivered at 30-week gestation by cesarean section because of severe hydrops. Fetal blood sampling revealed homozygous α-thalassemia. After immediate resuscitation, the infant was supported with frequent red cell transfusions. At 44 months of age, she received a 5 of 6 human leukocyte antigen-matched unrelated cord blood transplantation. She was treated with phlebotomy and chelation therapy with Deferasirox for correction of hemosiderosis and has been transfusion-independent since 41 days after transplant. She is currently 6 years after transplantation with stable, 100% donor engraftment, resolved iron overload, and normal growth and development.


Subject(s)
Cord Blood Stem Cell Transplantation , Homozygote , alpha-Thalassemia/genetics , alpha-Thalassemia/therapy , Blood Transfusion , Chelation Therapy , Child , Female , Humans , Iron Overload/etiology , Iron Overload/therapy , Phlebotomy , Treatment Outcome , alpha-Thalassemia/complications
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