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Updated: Aug 30, 2026

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Late-onset mitochondrial disorder with electromyographic evidence of myotonia
Mathew L P Howse1, Theresa M Wardell, Christopher J Fisher
1Department of Neurology, Middlesbrough General Hospital, Middlesbrough, Teeside, United Kingdom.
Abstract:
We describe a patient with chronic progressive external ophthalmoplegia (CPEO) due to a deletion of mitochondrial DNA (mtDNA) who had electromyographic evidence of myotonic discharges. Myotonia has not previously been described in association with mitochondrial disease and this report extends the known phenotypic expression of these disorders.
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