Abstract
Sickle cell anemia is a hereditary disorder in which the red blood cells, which function as the oxygen carriers throughout the body, develop in an abnormal manner. The red blood cells are normally disk-shaped and very flexible but in sickle cell patients the cells often become very rigid and crescent shaped. This abnormality in the shape and functionality of the red blood cells hinder the normal flow of blood in the body. The red blood cells are therefore rendered unable to move freely through the blood tissues and through organs that result in the failure of certain important organs ...
