47 top medical experts on Glycogen Storage Disease Type VII across 6 countries and 4 U.S. states, including 11 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- Glycogen Storage Disease Type VII: An autosomal recessive glycogen storage disease in which there is deficient expression of 6-phosphofructose 1-kinase in muscle (phosphofructokinase-1, muscle type) resulting in abnormal deposition of glycogen in muscle tissue. These patients have severe congenital muscular dystrophy and are exercise intolerant.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Broader Categories (#Experts): Glycogen Storage Disease (1,538), Muscular Dystrophies (1,543).
- Clinical Trials : at least 4 including 1 Active, 1 Completed
- Synonyms: Glycogenosis 7, Tarui Disease
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