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Up to: Disorder of glycolysis · Anemia due to erythrocyte enzyme disorder · Congenital nonspherocytic hemolytic anemia
Pyruvate kinase deficiency of red cells
A rare, genetic metabolic disorder due to pyruvate kinase deficiency characterized by a variable degree of chronic nonspherocytic hemolytic anemia resulting in a variable clinical manifestations ranging from fatal anemia at birth to a to a fully compensated hemolysis without apparent anemia.
This condition has no sub-types.