Glycogen Storage Disease :: Glycogen Storage Disease Type VII n Homeopathy

The phosphofructokinase enzyme is needed to facilitate the breakdown of glycogen into energy in muscle. Patients with this type of GSD have a deficient amount of this enzyme in their muscle tissue. With this deficiency, effective glycogen breakdown (glycolysis) during muscle stress cannot be accomplished, resulting in pain, weakness, and cramping in the exercising muscle.

Muscle Phosphofructokinase Deficiency
Tarui Disease

The clinical features of Type VII Glycogen Storage Disease are similar to those of Type V GSD. Patients experience early onset of fatigue and muscle pain with exercise. The body breaks down muscle when trying to attain energy, which causes many symptoms such as muscle pain, muscle cramping, muscle fatigue, and muscle tenderness. With the breakdown of muscle (rhabdomyolysis) and the release of the red protein myoglobin, myoglobinuria may develop, as evidenced by dark-red or red-brown urine. However, exercise intolerance is evident in childhood and symptoms are more severe than in Type V GSD.

Diagnosis of Type VII Glycogen Storage Disease is done by muscle biopsy, with a deficiency of the muscle phosphofructokinase enzyme and a modest accumulation of glycogen found. Patients may also display a hemolytic anemia.

Dr. Rajneesh Kumar Sharma
Homoeo Cure & Research Centre P. Ltd.
NH 74, Moradabad Road, Kashipur (Uttaranchal) 244713 India
Ph- 05947- 275535, 260327, 274338, 277418
Fax- 274338, 275535; Cells- 98 976 18594, 98 976 21896,

Spirit India