Glycogen Storage Disease Type VII

Also known as muscle phosphofructokinase deficiency or Tarui disease.

The clinical features of GSD VII are similar to those of GSD V with onset of more severe fatigue and muscle pain early in exercise. Symptoms are evident in childhood. GSD VII is caused by a deficiency of the phosphofructokinase enzyme which is needed to facilitate the breakdown of glucose into energy in muscle during exercise.

The body breaks down muscle (rhabdomyolysis) when trying to attain energy, which causes symptoms such as muscle pain, cramping, fatigue and tenderness. The red protein myoglobin is released and red-brown urine may be seen.

Diagnosis is by muscle biopsy, which will show a deficiency of muscle phosphofructokinase and a modest accumulation of glycogen. Patients may also display a hemolytic anemia. Treatment primarily consists of avoiding strenuous exercise. Some patients have been helped by a high protein diet. The enzyme deficiency is due to abnormalities in the muscle phosphofructokinase gene and is inherited as an autosomal recessive genetic disorder.

We do not currently have a Coordinator for GSD VII (a voluntary unpaid role.), but you can contact the AGSD-UK via the Contact us page.

• Support for people with GSD Type VII contacts, Facebook Group and more
• UK Clinic for GSD Type VII specialist clinic with multi-disciplinary team
• Coping with a rare genetic disorder - One woman’s story, as told to the Jewish News
• Information Cards - order these handy cards to help explain the disease
• Comprehensive article on Type VII - from Sweden
• OMIM entry on GSD Type VII (medical overview and reference to research)