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Congenital hemolytic anemia : ウィキペディア英語版 | Congenital hemolytic anemia
Congenital hemolytic anemia (or hereditary hemolytic anemia) refers to hemolytic anemia which is primarily due to congenital disorders. ==Types== Basically classified by causative mechanism, types of congenital hemolytic anemia include: *Genetic conditions of RBC Membrane * *Hereditary spherocytosis * *Hereditary elliptocytosis *Genetic conditions of RBC metabolism (enzyme defects). This group is sometimes called ''congenital nonspherocytic (hemolytic) anemia'', which is a term for a congenital hemolytic anemia without spherocytosis, and usually excluding hemoglobin abdormalities as well, but rather encompassing defects of glycolysis in the erythrocyte.〔(medconditions.net > Hemolytic Congenital, Nonspherocytic Anemia Definition ) Retrieved April 15, 2011〕 * *Glucose-6-phosphate dehydrogenase deficiency (G6PD or favism) * *Pyruvate kinase deficiency * *Aldolase A deficiency *Hemoglobinopathies/genetic conditions of hemoglobin * *Sickle cell anemia * *Congenital dyserythropoietic anemia * *Thalassemia
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