a project of the German Society of Anesthesiology and Intensive Care Medicine

 
 

Folder Mitochondrial disorders

Disease name: Mitochondrial Cytopathy, Mitochondrial Myopathy, Mitochondrial

Encephalomyopathy


ICD 10: G731.81

Synonyms: Mitochondrial diseases with typical combinations of clinical symptoms: Kearns-Sayre syndrom, progressive external ophthalmoplegia, Pearson syndrome, myoclonic epilepsy with ragged red fibers (MERFF), mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS), neuropathy with ataxia and retinitis pigmentosa, maternally inherited Leigh syndrome, Leber's hereditary optic neuropathy, Leigh disease, POLG1 associated disorders, mtDNA depletion syndromes

 

Citable version for download in the Journal A&I www.ai-online.info:

 

DOI: 10.19224/ai2017.s125


   
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