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Proximal myopathy with focal depletion of mitochondria

ORPHA:521305· ICD-10 G72.8

Definition

A rare genetic neuromuscular disease characterized by late onset of mild, progressive, proximal muscle weakness, severe myalgias during and after exercise, and susceptibility to rhabdomyolysis. Intellectual disability is mild or absent. There are no abnormalities of the skin. Muscle biopsy shows focal depletion of mitochondria especially at the center of muscle fibers, surrounded by enlarged mitochondria at the periphery.

Prevalence
<1 / 1 000 000
Inheritance
Mitochondrial inheritance
Age of onset
Adolescent, Adult, Childhood