thalassæmi
Thalassæmi, or thalassemia, is a group of inherited blood disorders caused by mutations that reduce or abolish the production of one of the hemoglobin (Hb) globin chains. The two main forms are alpha-thalassemia, due to mutations in the HBA1/HBA2 genes that lower α-globin synthesis, and beta-thalassemia, due to mutations in the HBB gene that limit β-globin production. The resulting imbalance in globin chain production leads to ineffective erythropoiesis and chronic hemolytic anemia. Thalassemias occur worldwide but are especially common in the Mediterranean, Middle East, Indian subcontinent, Southeast Asia, and parts of Africa.
Clinical features vary by type and severity. Individuals with mild thalassemia may be asymptomatic or have
Diagnosis typically starts with a complete blood count showing microcytic, hypochromic anemia. Iron studies help distinguish
Management is supportive and tailored to severity. Beta-thalassemia major often requires lifelong red cell transfusions and