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Alternate Name(s): Hereditary spherocytosis; Spherocytosis ...... Congenital spherocytic anemia is a disorder of the red blood cell membrane that leads to sphere-shaped red blood cells, and chronic hemolytic anemia (premature breakdown of red blood cells).
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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.
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Spherocytosis - Wikipedia, the free encyclopedia
Spherocytosis is an auto-hemolytic anemia (a disease of the blood) characterized by the production of red blood cells (RBCs), or erythrocytes , that are sphere-shaped, rather than bi-concave disk s...
en.wikipedia.org/wiki/Spherocytosis |
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Hereditary spherocytosis - Wikipedia, the free encyclopedia
Hereditary spherocytosis is a genetically-transmitted (autosomal dominant) form of spherocytosis, an auto-hemolytic anemia characterized by the production of red blood cells that are sphere-shaped ra...
en.wikipedia.org/wiki/Hereditary_spherocytosis |
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Online Medical Dictionary and glossary with medical definitions ... Hereditary spherocytosis: A genetic disorder of the red blood cell membrane clinically characterized by anemia, jaundice (yellowing) and splenomegaly (enlargement of the spleen).
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What is hereditary spherocytosis? Hereditary spherocytosis (HS) is an inherited disease that causes anemia. If your child has hereditary spherocytosis, either parent may also have the disease. Occasionally, neither parent of an affected child has the disease;
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Hereditary spherocytosis; Spherocytosi ... Having a family history of spherocytosis increases the risk for this disorder. ... Red blood cells, spherocytosis...
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Hereditary spherocytosis and hereditary elliptocytosis are congenital RBC membrane disorders. Symptoms, generally milder in hereditary elliptocytosis, include variable degrees of anemia, jaundice, and splenomegaly.
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Overview: Hereditary spherocytosis (HS) is a familial hemolytic disorder with marked heterogeneity of clinical features, ranging from an asymptomatic condition to fulminant hemolytic anemia. The morphologic hallmark of HS is the microspherocyte, which is caused by loss ... ... More on Spherocytosis, Hereditary...
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