Sickle cell anemia with malaria: a rare case report.

Sickle cell disease is the prototype of hereditary hemoglobinopathies, characterized by the production of structurally abnormal hemoglobin. Sickle cell anemia results from a point mutation that leads to substitution of valine for glutamic acid at the sixth position of the β globin chain. We report a young male admitted with fever and weakness for 3 days. Hematological test reveals Plasmodium falciparum malaria parasite and sickle cell anemia. Patient was treated and get cured from malaria and discharged.