Thalassemia

Created using ChatSlide

Thalassemia is a genetic blood disorder characterized by mutated hemoglobin production, affecting millions worldwide. The condition varies in severity, with significant socio-economic implications due to healthcare demands. Genetic inheritance plays a crucial role, with specific mutations elevating risk factors. Common symptoms include fatigue and anemia, making early diagnosis vital through specific tests. Treatment often involves regular blood transfusions and iron chelation therapy, though...