Définition:
An autosomal recessive glycogen storage disease in which there is deficient expression of 6-phosphofructose 1-kinase in muscle () resulting in abnormal deposition of glycogen in muscle tissue. These patients have severe congenital muscular dystrophy and are exercise intolerant.
Synonyme(s):
Glycogénose de type 7 /
Maladie de Tarui /
Déficit en phosphofructokinase musculaire /