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Cortical reflex myoclonus in patients with the mitochondrial DNA transfer RNALys(8344) (MERRF) mutation

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Abstract

Five patients from three families with the syndrome of myoclonic epilepsy and ragged red fibres (MERRF), associated with the mitochondrial DNA point mutation at position 8344, were studied neurophysiologically to determine the characteristics of their myoclonus. The findings were those of cortical reflex myoclonus, with enlarged cortical somatosensory evoked potentials and late reflex responses to peripheral nerve stimulation. Electroencephalography showed paroxysmal spike and polyspike and wave discharges, with photic sensitivity. This pattern of electrophysiological abnormalities was uniform, despite considerable variation in severity of myoclonus. Although a consistent finding, cortical reflex myoclonus is not specific to MERRF amongst myoclonic syndromes.

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Authors and Affiliations

  1. Human Movement and Balance Unit, Institute of Neurology, Queen Square, WClN 313G, London, UK

    P. D. Thompson

  2. Neurogenetics Section, Department of Clinical Neurology, Institute of Neurology, Queen Square, WCIN 313G, London, UK

    S. R. Hammans & A. E. Harding

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  1. P. D. Thompson
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  2. S. R. Hammans
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  3. A. E. Harding
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Thompson, P.D., Hammans, S.R. & Harding, A.E. Cortical reflex myoclonus in patients with the mitochondrial DNA transfer RNALys(8344) (MERRF) mutation. J Neurol 241, 335–340 (1994). https://doi.org/10.1007/BF00868443

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  • DOI: https://doi.org/10.1007/BF00868443

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