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Journal of Evidence Based Medicine and Healthcare
We report here a patient from upper Assam region of India with Hb E/β thalassemia disease, whose father belongs to the tea garden community and mother is Assamese where Hb E is very common. The patient was suffering from severe anaemia and hepatosplenomegaly. After examination two units of blood transfusion and folic acid course were given to the patient. Patient was finally treated with chelation therapy.doi:10.18410/jebmh/2015/191 fatcat:oliu5mrdjvftjkbhonzzsfmara