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  • noun

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any pathology of the muscles that is not attributable to nerve dysfunction

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Skeletal muscle magnetic resonance imaging of the lower limbs in late-onset lipid storage myopathy with electron transfer flavoprotein dehydrogenase gene mutations.
Lipid storage myopathy has a relatively short differential diagnosis and includes primary carnitine deficiency, multiple acyl-CoA dehydrogenase deficiency (MADD, otherwise known as glutaric aciduria type II) and neutral lipid storage disorders (2).
Late-onset lipid storage myopathy (LSM) is an autosomal recessive muscular disorder associated with errors of fatty acid, amino acid, and choline metabolism.
The latter is the most common form of lipid storage myopathy in China.
Fulminant lipid storage myopathy due to multiple acyl-coenzyme a dehydrogenase deficiency.