Mitochondrial myopathies. Clinical, morphological and biochemical aspects

MeSH terms

• Adolescent
• Adult
• Central Nervous System Diseases / etiology
• Child
• Child, Preschool
• Cytochrome b Group / deficiency
• Cytochrome-c Oxidase Deficiency
• Female
• Genes
• Humans
• Infant
• Infant, Newborn
• Male
• Metabolism, Inborn Errors / complications
• Metabolism, Inborn Errors / genetics
• Metabolism, Inborn Errors / metabolism*
• Metabolism, Inborn Errors / therapy
• Mitochondria, Muscle / metabolism*
• Mitochondria, Muscle / ultrastructure
• Muscular Diseases / complications
• Muscular Diseases / metabolism*
• Muscular Diseases / pathology
• Muscular Diseases / therapy
• NAD(P)H Dehydrogenase (Quinone)
• Ophthalmoplegia / etiology
• Pyruvate Dehydrogenase Complex Deficiency Disease
• Quinone Reductases / deficiency