Lifelong management is required; cure may be possible with bone marrow transplant
Beta thalassemia is a genetic blood disorder characterized by reduced or absent production of beta-globin chains, leading to anemia. Treatment may include blood transfusions, iron chelation therapy, and, in severe cases, bone marrow transplantation.
Inherited blood disorder affecting hemoglobin synthesis
Anemia, fatigue, growth delay
Genetic testing, blood tests
Variable; depends on the type and severity of thalassemia
Anemia, complications in severe cases
Genetic mutations
Blood transfusions, iron chelation, bone marrow transplant
Blood transfusions, iron chelation, bone marrow transplant
Genetic disorder affecting hemoglobin production
Individualized care based on the type and severity of thalassemia
Remember, the information provided here is intended for general knowledge purposes and may not apply to every individual case. To ensure you have accurate information relevant to your specific situation, always consult with a healthcare professional.
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