Sickle beta thalassemia is a genetic condition that results in a mild form of sickle cell anemia and causes abnormal production of hemoglobin. Symptoms include mild anemia, weakness, tiredness, occasional pain and stiffness in the back, arms, and legs, clots in the blood vessels, a higher risk of infection, and an enlarged spleen. Treatment involves the drug hydroxyurea, blood transfusions, and bone marrow transplants.
Hello, Welcome to icliniq.com. As per your description, your friend seems to be having sickle beta-thalassemia.
Hello, Welcome to icliniq.com. I have seen the reports (attachment removed to protect patient identity). Thalassemia and sickle cell anemia are autosomal recessive disorders.
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