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       <title>Mitochondrial disorders - OrphanAnesthesia</title>
       <description><![CDATA[<p><strong>Disease name:&nbsp;</strong>Mitochondrial Cytopathy, Mitochondrial Myopathy, Mitochondrial</p>

<div>Encephalomyopathy</div>

<p><br />
<strong>ICD 10:&nbsp;</strong>G731.81<br />
<br />
<strong>Synonyms:&nbsp;</strong>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</p>

<p>&nbsp;</p>

<h6>Citable version for download in the Journal A&amp;I <a href="http://www.ai-online.info" target="_blank">www.ai-online.info</a>:</h6>

<p>&nbsp;</p>

<p><a class="doi-button" href="https://doi.org/10.19224/ai2017.s125" target="_blank">DOI: 10.19224/ai2017.s125</a></p>]]></description>
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