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J Pediatr ; 154(5): 766-8, 2009 May.
Article in English | MEDLINE | ID: mdl-19364562

ABSTRACT

Recently, intrauterine transfusions and hematopoietic cell transplantation (HCT) have changed homozygous alpha-thalassemia from a frequently fatal disease to a potentially survivable condition. We present a patient with Hemoglobin Bart's disease who was cured after failing to engraft with 1 unrelated HCT, but engrafting after a second unrelated donor HCT.


Subject(s)
Blood Transfusion, Intrauterine , Fetal Diseases/therapy , Hematopoietic Stem Cell Transplantation , Hemoglobins, Abnormal , alpha-Thalassemia/therapy , Chimerism , Developmental Disabilities/etiology , Erythrocyte Transfusion , Female , Fetal Diseases/blood , Fetal Diseases/genetics , Graft Survival , Humans , Infant, Newborn , Male , Pregnancy , Prenatal Diagnosis , Tissue Donors , alpha-Thalassemia/genetics
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