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Sickle cell anemia and its acute complications in patients

Ibrahim Khan

Sickle cell anemia is an inherited disorder of the globin chains that causes hemolysis and chronic organ damage. Sickle cell anemia is the most widely recognized type of sickle cell disease (SCD), with a long lasting hardship of hemolytic weakness requiring blood transfusions, pain crises, and organ damage. Starting from the primary portrayal of the unpredictable sickle-shaped red blood cells (RBC) over a long time back, how we might interpret the illness has developed massively. On-going advances in the field, all the more so inside the most recent thirty years, have mitigated side effects for endless patients, particularly in major league salary nations. This movement audits the pathophysiology, show, entanglements, determination, and therapy of sickle cell anemia and furthermore features the job of the interprofessional group in the administration of these patients.