Cardiopulmonary bypass graft in a post COVI-19 thalassemic patient
Thalassemia is of the most frequent haemoglobinopathy that includes a heterogeneous group of inherited autosomal recessive pathologies caused by defective synthesis of globin subunit that comprise haemoglobin production. In β-thalassemia, insufficient quantities of β-globin chains are produced, causing ineffective erythropoiesis and microcytic hypochromic anaemia.
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