Preferred Label : mitochondrial encephalomyopathies;

MeSH definition : A heterogenous group of disorders characterized by alterations of mitochondrial metabolism that result in muscle and nervous system dysfunction. These are often multisystemic and vary considerably in age at onset (usually in the first or second decade of life), distribution of affected muscles, severity, and course. (From Adams et al., Principles of Neurology, 6th ed, pp984-5);

MeSH synonym : encephalomyopathies, mitochondrial; encephalomyopathy, mitochondrial; mitochondrial encephalomyopathy;

MeSH annotation : GEN or unspecified; prefer specifics; coord with specific dysfunction if pertinent; DF: MITOCHONDRIAL ENCEPH; GEN or unspecified; prefer specifics; coord with specific dysfunction if pertinent; general or unspecified; prefer specifics; coordinate with specific dysfunction if pertinent;

Wikipedia link : https://en.wikipedia.org/wiki/Mitochondrial encephalomyopathy;

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A heterogenous group of disorders characterized by alterations of mitochondrial metabolism that result in muscle and nervous system dysfunction. These are often multisystemic and vary considerably in age at onset (usually in the first or second decade of life), distribution of affected muscles, severity, and course. (From Adams et al., Principles of Neurology, 6th ed, pp984-5)

http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=166105
2011
France
scientific and technical information
mitochondrial encephalomyopathies

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http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=255235
2011
France
scientific and technical information
DNA, A-form
mitochondrial encephalomyopathies
DNA, mitochondrial

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http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=238329
2011
France
scientific and technical information
oxidative phosphorylation
mitochondrial encephalomyopathies

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26/04/2025


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