Mitochondrial myopathy with diabetes
Other Names: Mitochondrial myopathy, lipid type A rare, genetic, mitochondrial DNA-related mitochondrial myopathy disorder characterized by slowly progressive muscular weakness (proximal greater than distal), predominantly involving the facial muscles and scapular girdle, associated with insulin-dependent diabetes mellitus. Neurological involvement and congenital myopathy may be variably observed.
NIH genetic and rare disease info[edit source]
Mitochondrial myopathy with diabetes is a rare disease.
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