Hematopoietic Stem Cell Transplantation for Thalassemia

Thalassemia is an autosomal recessive disorder associated with defective synthesis of the α- or β-chain of hemoglobin. For β-thalassemia major patients, therapeutic options are either monthly red cell transfusions and chelation therapy or allogeneic stem cell transplant. Stem cell transplant is the...

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Bibliographic Details
Main Author: Ali Ghasemi
Format: Article
Language:English
Published: Mashhad University of Medical Sciences 2014-05-01
Series:International Journal of Pediatrics
Subjects:
Online Access:http://ijp.mums.ac.ir/pdf_2672_192310b62664ea420e9bb0e9f448d111.html