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Beta-thalassemia is a hereditary blood disorder characterized by reduced or absent synthesis of beta chains of hemoglobin, leading to varying degrees of anemia and related complications. It includes three main forms: thalassemia major, which requires regular blood transfusions; thalassemia intermedia, which presents later with milder symptoms; and thalassemia minor, which is usually asymptomatic. Diagnosis is based on hematologic and genetic testing, and treatment options include transfusions, iron chelatio

Author

Hamza Pervaiz

Language

EN