Thalassemia is a genetic condition that affects the production of hemoglobin, resulting in severe anemia. There are two different types of thalassemia: alpha and beta. Alpha-thalassemia involves genetic changes in two genes (HBA1 and HBA2). Beta-thalassemia involves changes in one gene (HBB). Thalassemia also classified as thelassemia major and thalassemia minor.
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