Abstract
Mitochondrial disorders are a heterogeneous group of disorders resulting from primary dysfunction of the respiratory chain. Muscle tissue is highly metabolically active, and therefore myopathy is a common element of the clinical presentation of these disorders, although this may be overshadowed by central neurological features. This review is aimed at a general medical and neurologist readership and provides a clinical approach to the recognition, investigation, and treatment of mitochondrial myopathies. Emphasis is placed on practical management considerations while including some recent updates in the field. © 2013 Informa UK, Ltd.
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CITATION STYLE
Pfeffer, G., & Chinnery, P. F. (2013, February). Diagnosis and treatment of mitochondrial myopathies. Annals of Medicine. https://doi.org/10.3109/07853890.2011.605389
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