Isolated Mitochondrial Myopathy

Isolated Mitochondrial Myopathy, also known as autosomal dominant mitochondrial myopathy with exercise intolerance, is related to myopathy, isolated mitochondrial, autosomal dominant and myopathy, and has symptoms including facial paresis An important gene associated with Isolated Mitochondrial Myopathy is CHCHD10 (Coiled-Coil-Helix-Coiled-Coil-Helix Domain Containing 10). Related phenotypes are short stature and proximal muscle weakness in lower limbs