Construct · 1 fields · 2 citations
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In hematology, sickling is the process by which red blood cells deform from their normal flexible disc into a rigid, elongated crescent or sickle shape. In sickle cell disease it occurs when abnormal haemoglobin S polymerises under low oxygen, distorting the cell; the stiffened cells obstruct small vessels and are destroyed early, causing pain crises and anaemia. Herrick's 1910 case report first described the sickle-shaped cells, and Pauling and colleagues' Sickle cell anemia, a molecular disease traced the defect to the haemoglobin molecule. The referent is a pathological cell deformation, unrelated to a dancer's foot beyond the crescent shape both are named for.[1][2]
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