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Sickle cell anemia is an inherited blood disorder in which the red blood cells become misshapen and break down more easily than normal cells. This leads to reduced oxygen flow to tissues and organs, causing episodes of severe pain, fatigue, and other complications. It primarily affects people of African descent, but can also occur in individuals of Hispanic, Middle Eastern and Mediterranean backgrounds. There is currently no cure for sickle cell anemia, but treatments include pain management, blood transfusions, and sometimes bone marrow transplants.
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