Thalassemias are inherited autosomal recessive hematologic disorders where there is a mutation(s) for the synthesis of hemoglobin chain(s) (1). Hemoglobin consists of a heme ring with four globin chains. With alpha (α) thalassemia the α-globin chains are either decreased or absent resulting in an excess of unpaired beta (β) globin chains. With β-thalassemia the β-globin chains are decreased or absent resulting in an excess of α-globin chains. The excess unpaired globin chains leads to hemolysis