Thalassemia is a genetic hemolytic anemia. The disease mechanism affects the synthesis of globin chains in patients [1,2]. The cause of thalassemia is the unbalanced production of globin chains, resulting in ineffective erythropoiesis and increased hemolysis. While the carrier of the gene may not have symptoms, patients with severe thalassemia require regular blood transfusions and…
Thalassemia treatment using umbilical stem cells






