Type 7 glycogen storage disease; marked by exercise intolerance in childhood, hemolysis, and hyperuricemia. Deficiency is in M isoenzyme of phosphofructokinase, with complete absence in muscle and partial deficiency in blood.
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Type 7 glycogen storage disease; marked by exercise intolerance in childhood, hemolysis, and hyperuricemia. Deficiency is in M isoenzyme of phosphofructokinase, with complete absence in muscle and partial deficiency in blood.