Definition for Sickle-cell anemia

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1) A disease caused by a genetic mutation in a hemoglobin gene in which sickle-shaped red blood cells are less able to move smoothly through capillaries and can block blood flow, resulting in severe pain and cell death of the surrounding tissue.

2) A genetic disorder in which erythrocytes take on an abnormal curved or “sickle” shape. These cells are fragile and are easily damaged, leading to a hemolytic anemia.

3) A recessive genetic disorder associated with an abnormal type of hemoglobin, a blood transport protein.