Literature DB >> 8006688

Cortical reflex myoclonus in patients with the mitochondrial DNA transfer RNA(Lys)(8344) (MERRF) mutation.

P D Thompson1, S R Hammans, A E Harding.   

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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Year:  1994        PMID: 8006688     DOI: 10.1007/BF00868443

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


  25 in total

1.  Mitochondrial encephalopathies: molecular genetic diagnosis from blood samples.

Authors:  S R Hammans; M G Sweeney; M Brockington; J A Morgan-Hughes; A E Harding
Journal:  Lancet       Date:  1991-06-01       Impact factor: 79.321

2.  A MERRF/MELAS overlap syndrome associated with a new point mutation in the mitochondrial DNA tRNA(Lys) gene.

Authors:  M Zeviani; F Muntoni; N Savarese; G Serra; V Tiranti; F Carrara; C Mariotti; S DiDonato
Journal:  Eur J Hum Genet       Date:  1993       Impact factor: 4.246

3.  [An autopsy case of degenerative type myoclonus epilepsy associated with Friedreich's ataxia and mitochondrial myopathy (author's transl)].

Authors:  T Nakano; H Sakai; N Amano; S Yagishita; Y Ito
Journal:  No To Shinkei       Date:  1982-04

4.  Myoclonus epilepsy and ragged-red fibres (MERRF). 2. Electrophysiological studies and comparison with other progressive myoclonus epilepsies.

Authors:  N So; S Berkovic; F Andermann; R Kuzniecky; D Gendron; L F Quesney
Journal:  Brain       Date:  1989-10       Impact factor: 13.501

5.  On the significance of giant somatosensory evoked potentials in cortical myoclonus.

Authors:  J C Rothwell; J A Obeso; C D Marsden
Journal:  J Neurol Neurosurg Psychiatry       Date:  1984-01       Impact factor: 10.154

6.  [Spinocerebellar degeneration, optic atrophy, epilepsy, myoclonus and mitochondrial myopathy: a case report (author's transl)].

Authors:  J Roger; J F Pellissier; C Dravet; M Bureau-Paillas; M Arnoux; J L Larrieu
Journal:  Rev Neurol (Paris)       Date:  1982       Impact factor: 2.607

7.  A tRNA(Lys) mutation in the mtDNA is the causal genetic lesion underlying myoclonic epilepsy and ragged-red fiber (MERRF) syndrome.

Authors:  A S Noer; H Sudoyo; P Lertrit; D Thyagarajan; P Utthanaphol; R Kapsa; E Byrne; S Marzuki
Journal:  Am J Hum Genet       Date:  1991-10       Impact factor: 11.025

8.  Myoclonus, cerebellar disorder, neuropathy, mitochondrial myopathy, and ACTH deficiency.

Authors:  H Sasaki; S Kuzuhara; I Kanazawa; T Nakanishi; T Ogata
Journal:  Neurology       Date:  1983-10       Impact factor: 9.910

9.  Myoclonus epilepsy associated with ragged-red fibres (mitochondrial abnormalities ): disease entity or a syndrome? Light-and electron-microscopic studies of two cases and review of literature.

Authors:  N Fukuhara; S Tokiguchi; K Shirakawa; T Tsubaki
Journal:  J Neurol Sci       Date:  1980-07       Impact factor: 3.181

10.  The spectrum of cortical myoclonus. From focal reflex jerks to spontaneous motor epilepsy.

Authors:  J A Obeso; J C Rothwell; C D Marsden
Journal:  Brain       Date:  1985-03       Impact factor: 13.501

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  1 in total

Review 1.  Movement disorders in mitochondrial disease.

Authors:  Roula Ghaoui; Carolyn M Sue
Journal:  J Neurol       Date:  2018-01-06       Impact factor: 4.849

  1 in total

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