Hereditary spherocytosis is a genetic condition affecting the red blood cells, characterized by destruction of the red blood cells in the spleen, yellow discoloration of the skin, and enlargement of the spleen. The cause of the condition is a genetic defect that is transferred from parents to children. The diagnosis of hereditary spherocytosis is made on the basis of peripheral blood smear examination, red cell fragility test, etc. The treatment of the condition includes blood transfusion, folic acid supplements, and partial or complete removal of the spleen.
Hereditary Spherocytosis: Abnormally Morphed RBCs
Hereditary spherocytosis is a genetic disorder that affects red blood cells and causes hemolytic anemia. Read to know more about hereditary spherocytosis.
