الفهرس 
?-thalassemia
Complications of ?-TMOnly 14 pages are availabe for public view
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Abstract
.β-thalassemias are a group of recessively inherited hemoglobin disorders characterized by reduced synthesis of β globin chains. Thalassemia constitutes the most common inherited recessive disorder associated with consanguinity, which is a common phenomenon in Egypt. Allo-HSCT is the only established treatment modality that provides a possibility of cure and
considered cost effective compared with conventional therapy. Current
results of transplantation in pediatrics from matched related donors offer
80% to 87% probability of cure according to risk classes. The thalassemia
free survival was respectively 85–90% for class I, 80% for class II, and 70%
for class III, while the TRM increased from class I to III.