What Is MYH7-Related Scapuloperoneal Myopathy?
Source: Genetic and Rare Diseases (GARD) Information Center
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MYH7-Related Scapuloperoneal Myopathy
MYH7-related Late-onset Scapuloperoneal Muscular Dystrophy; MYH7-related Late-onset SPMD
MYH7-related scapuloperoneal myopathy is an inherited muscular dystrophy characterized by weakness and wasting of the muscles in the lower legs and the area of the shoulder blades. Explore symptoms, causes, and genetics of this rare condition.
Muscular Dystrophy - NICHD
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Myopathy is associated with mitochondrial disease and often leads to exercise intolerance, cramps, and fatigue
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Source: Genetic and Rare Diseases (GARD) Information Center
Mutation
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Source: Genetic and Rare Diseases (GARD) Information Center
physical therapy
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Source: Genetic and Rare Diseases (GARD) Information Center
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