Definition: a group of diverse hereditary disorders caused by genetic mutation of mitochrondrial DNA; includes ragged red fiber myopathy; progressive external ophthalmoplegia; Leigh syndrome; myoclonic epilepsy with ragged red fiber myopathy (MERRF); mitochondrial myopathy, encephalopathy, lactic cidosis, and stroke (MELAS); and Lieber optic neuropathy.
Disclaimer: This site is designed to offer information for general educational purposes only. The health information furnished on this site and the interactive responses are not intended to be professional advice and are not intended to replace personal consultation with a qualified physician, pharmacist, or other healthcare professional. You must always seek the advice of a professional for questions related to a disease, disease symptoms, and appropriate therapeutic treatments.
Search Stedman's Medical Dictionary
Examples: glitazone, GI cocktail, etc.
© Copyright 2017 Wolters Kluwer. All Rights Reserved. Review Date: Sep 19, 2016.