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Red blood cells ( sickle cell, elliptocytosis , spherocytosis , multiple sickle cells , Ovalocytoses , sickle and pappenheimer , target cells )


Red blood cells, sickle cell



Sickle cell anemia is an inherited blood disease in which the red blood cells produce abnormal pigment (hemoglobin). The abnormal hemoglobin causes deformity of the red blood cells into crescent or sickle-shapes, as seen in this photomicrograph.


                   Red blood cells, elliptocytosis 




Elliptocytosis is a hereditary disorder of the red blood cells (RBCs). In this condition, the RBCs assume an elliptical shape, rather than the typical round shape.


Red blood cells, spherocytosis 



Spherocytosis is a hereditary disorder of the red blood cells (RBCs), which may be associated with a mild anemia. Typically, the affected RBCs are small, spherically shaped, and lack the light centers seen in normal, round RBCs.


Red blood cells, multiple sickle cells 



Sickle cell anemia is an inherited disorder in which abnormal hemoglobin (the red pigment inside red blood cells) is produced. The abnormal hemoglobin causes red blood cells to assume a sickle shape, like the ones seen in this photomicrograph.


Ovalocytoses 



Red blood cells (RBCs) are normally round. In ovalocytosis, the cells are oval. Other conditions that produce abnormally shaped RBCs include spherocytosis and eliptocytosis.


Red blood cells, sickle cells 


These crescent or sickle-shaped red blood cells (RBCs) are present with Sickle cell anemia, and stand out clearly against the normal round RBCs. These abnormally shaped cells may become entangled and block blood flow in the small blood vessels (capillaries).



Red blood cells, sickle and pappenheimer


This photomicrograph of red blood cells (RBCs) shows both sickle-shaped and pappenheimer bodies.


Red blood cells, target cells




These abnormal red blood cells (RBCs) resemble targets. These cells are seen in association with some forms of anemia, and following the removal of the spleen (splenectomy).  





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