Abstract
Drepanocytosis (or sickle cell anemia) is a hereditary disease which is largely confined to black people. In the red cells of patients who suffer from this condition, normal hemoglobin (A) is replaced by an abnormal hemog lobi n (S). When the oxygen tension decreases (for instance at high altitude), the hemoglobin molecules polymerize and form tiny, long rods inside the cell. These small rods of hemoglobin cluster into sheaf-like bundles which stretch the membrane and deform the discocyte. Such cells appear sickle-shaped.
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© 1974 Springer-Verlag Berlin Heidelberg
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Bessis, M. (1974). Drepanocytes. In: Corpuscles. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-65657-6_5
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DOI: https://doi.org/10.1007/978-3-642-65657-6_5
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-642-65659-0
Online ISBN: 978-3-642-65657-6
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