Definição:
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.
Sinônimos:
doenassa de tarui /
doenassa do armazenamento de glicogaanio tipo vii /
glicogenose 7 /