| type V |
muscle phosphorylase deficiency: an autosomal recessive disorder caused by a defect in the skeletal muscle isozyme of glycogen phosphorylase; it is characterized by muscle cramps and fatigue during exercise.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
|---|---|
| type VI |
hepatic phosphorylase deficiency: an autosomal recessive disorder caused by deficiency of the liver isozyme of glycogen phosphorylase; it is characterized by hepatomegaly, mild to moderate hypoglycemia, and mild ketosis. Phosphorylase b kinase deficiency was previously included in this type by some authors.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
| type VII |
muscle phosphofructokinase deficiency: an autosomal recessive disorder caused by deficiency of the muscle isozyme of 6-phosphofructokinase; it is characterized by muscle weakness and cramping after exercise. Activity of the erythrocyte isozyme is also decreased, causing increased hemolysis.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
| type VIII |
phosphorylase b kinase deficiency.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|