08/05/2023
Thalassemia is an inherited blood disorder that affects the production of hemoglobin, the protein in red blood cells that carries oxygen throughout the body. People with thalassemia have a reduced ability to produce hemoglobin, which can lead to anemia and a range of health complications. There are two main types of thalassemia: alpha thalassemia and beta thalassemia, and their severity varies from mild to life-threatening. Symptoms may include fatigue, weakness, pale skin, jaundice, and bone deformities. Treatment may involve blood transfusions, iron chelation therapy, and in severe cases, bone marrow transplantation.
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