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Thalassemia is an autosomal recessive blood disorder that primarily affects people from Mediterranean ethnic groups. Thalassemia minor may cause no symptoms, while thalassemia major develops in childhood and is a life-threatening disease characterized by anemia and excessive iron absorption from frequent blood transfusions. Treatment for thalassemia major involves regular blood transfusions combined with chelation therapy to remove excess iron from the body in order to prevent cardiac complications, which a
- Author
- Tanya
- Language
- EN