
Deficiency of Coenzyme Q10 (CoQ10) in muscle has been associated with a spectrum of diseases including infantile-onset multi-systemic diseases, encephalomyopathies with recurrent myobinuria, cerebellar ataxia, and pure myopathy. CoQ10 deficiency predominantly affects children, but patients have presented with adult-onset cerebellar ataxia or myopathy. Mutations in the CoQ10 biosynthetic genes, COQ2 and PDSS2, have been identified in children with the infantile form of CoQ10 deficiency; however, the molecular genetic bases of adult-onset CoQ10 deficiency remains undefined.
Adult, Male, Cerebellar Ataxia, Ubiquinone, Muscles, Middle Aged, Models, Biological, Electron Transport, Models, Chemical, Muscular Diseases, Mitochondrial Encephalomyopathies, Humans, Female, Muscle, Skeletal
Adult, Male, Cerebellar Ataxia, Ubiquinone, Muscles, Middle Aged, Models, Biological, Electron Transport, Models, Chemical, Muscular Diseases, Mitochondrial Encephalomyopathies, Humans, Female, Muscle, Skeletal
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