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Section 6 - Myoclonus

Published online by Cambridge University Press:  04 July 2017

Kailash P. Bhatia
Affiliation:
Institute of Neurology, University College London
Roberto Erro
Affiliation:
Università degli Studi di Salerno, Italy
Maria Stamelou
Affiliation:
University of Athens, Greece
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Summary

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Chapter
Information
Case Studies in Movement Disorders
Common and Uncommon Presentations
, pp. 116 - 133
Publisher: Cambridge University Press
Print publication year: 2017

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References

Suggested Readings

Nardocci, N. Myoclonus-dystonia syndrome. Handb Clin Neurol. 2011;100:563–75.CrossRefGoogle ScholarPubMed
Quinn, NP. Essential myoclonus and myoclonic dystonia. Mov Disord. 1996;11:119–24.CrossRefGoogle ScholarPubMed
Roze, E, Apartis, E, Clot, F et al. Myoclonus-dystonia: clinical and electrophysiologic pattern related to SGCE mutations. Neurology. 2008;70:1010–16.CrossRefGoogle ScholarPubMed

Suggested Readings

Chew, NK, Mir, P, Edwards, MJ, et al. The natural history of Unverricht-Lundborg disease: a report of eight genetically proven cases. Mov Disord. 2008;23:107–13.CrossRefGoogle ScholarPubMed
Kälviäinen, R, Khyuppenen, J, Koskenkorva, P, Eriksson, K, Vanninen, R, Mervaala, E. Clinical picture of EPM1-Unverricht-Lundborg disease. Epilepsia. 2008;49:549–56.CrossRefGoogle ScholarPubMed

Suggested Readings

Boissé Lomax, L, Bayly, MA, Hjalgrim, H, et al. ‘North Sea’ progressive myoclonus epilepsy: phenotype of subjects with GOSR2 mutation. Brain. 2013;136:1146–54.CrossRefGoogle ScholarPubMed
Corbett, MA, Schwake, M, Bahlo, M, et al. A mutation in the Golgi Qb-SNARE gene GOSR2 causes progressive myoclonus epilepsy with early ataxia. Am J Hum Genet. 2011;88:657–63.CrossRefGoogle ScholarPubMed
van Egmond, ME, Verschuuren-Bemelmans, CC, Nibbeling, EA, et al. Ramsay Hunt syndrome: clinical characterization of progressive myoclonus ataxia caused by GOSR2 mutation. Mov Disord. 2014;29:139–43.CrossRefGoogle ScholarPubMed

Suggested Readings

Bhatia, KP, Brown, P, Gregory, R, et al. Progressive myoclonic ataxia associated with coeliac disease. The myoclonus is of cortical origin, but the pathology is in the cerebellum. Brain. 1995;118:1087–93.CrossRefGoogle ScholarPubMed
Ganos, C, Kassavetis, P, Erro, R, Edwards, MJ, Rothwell, J, Bhatia, KP. The role of the cerebellum in the pathogenesis of cortical myoclonus. Mov Disord. 2014;29:437–43.CrossRefGoogle ScholarPubMed
Lu, CS, Thompson, PD, Quinn, NP, Parkes, JD, Marsden, CD. Ramsay Hunt syndrome and coeliac disease: a new association? Mov Disord. 1986;1:209–19.CrossRefGoogle ScholarPubMed

Suggested Readings

Katschnig, P, Massano, J, Edwards, MJ, Schwingenschuh, P, Cordivari, C, Bhatia, KP. Late-onset asymmetric myoclonus: an emerging syndrome. Mov Disord. 2011;26:1744–8.CrossRefGoogle ScholarPubMed
Stamelou, M, Alonso-Canovas, A, Bhatia, KP. Dystonia in corticobasal degeneration: a review of the literature on 404 pathologically proven cases. Mov Disord. 2012;27:696702.CrossRefGoogle ScholarPubMed
Thompson, PD, Day, BL, Rothwell, JC, Brown, P, Britton, TC, Marsden, CD. The myoclonus in corticobasal degeneration. Evidence for two forms of cortical reflex myoclonus. Brain. 1994;117:1197–207.CrossRefGoogle ScholarPubMed

Suggested Readings

Corato, M, Cereda, C, Cova, E, Ferrarese, C, Ceroni, M. Young-onset CJD: age and disease phenotype in variant and sporadic forms. Funct Neurol. 2006;21:211–15.Google ScholarPubMed
Day, GS, Tang-Wai, DF. When dementia progresses quickly: a practical approach to the diagnosis and management of rapidly progressive dementia. Neurodegener Dis Manag. 2014;4:4156.CrossRefGoogle Scholar
Takada, LT, Geschwind, MD. Prion diseases. Semin Neurol. 2013;33:348–56.CrossRefGoogle ScholarPubMed

Suggested Readings

Cen, Z, Huang, C, Yin, H, et al. Clinical and neurophysiological features of familial cortical myoclonic tremor with epilepsy. Mov Disord. 2016;31:17041710.CrossRefGoogle ScholarPubMed
Gao, L, Li, L, Ye, J, et al. Identification of a novel mutation in PLA2G6 gene in a Chinese pedigree with familial cortical myoclonic tremor with epilepsy. Seizure. 2016;41:81–5.CrossRefGoogle Scholar
Martí-Massó, JF, Bergareche, A, Makarov, V, et al. The ACMSD gene, involved in tryptophan metabolism, is mutated in a family with cortical myoclonus, epilepsy, and parkinsonism. J Mol Med (Berl). 2013;91:1399–406.CrossRefGoogle Scholar
Stogmann, E, Reinthaler, E, Eltawil, S, et al. Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2. Brain. 2013;136:1155–60.CrossRefGoogle ScholarPubMed
van Rootselaar, AF, van Schaik, IN, van den Maagdenberg, AM, et al. Familial cortical myoclonic tremor with epilepsy: a single syndromic classification for a group of pedigrees bearing common features. Mov Disord. 2005;20:665–73.CrossRefGoogle ScholarPubMed

Suggested Readings

Okuma, Y, Fujishima, K, Miwa, H, Mori, H, Mizuno, Y. Myoclonic tremulous movements in multiple system atrophy are a form of cortical myoclonus. Mov Disord. 2005;20:451–6.CrossRefGoogle ScholarPubMed
Salazar, G, Valls-Solé, J, Martí, MJ, Chang, H, Tolosa, ES. Postural and action myoclonus in patients with parkinsonian type multiple system atrophy. Mov Disord. 2000;15:7783.3.0.CO;2-N>CrossRefGoogle ScholarPubMed
Wenning, GK, Ben Shlomo, Y, Magalhães, M, Daniel, SE, Quinn, NP. Clinical features and natural history of multiple system atrophy. An analysis of 100 cases. Brain. 1994;117:835–45.CrossRefGoogle ScholarPubMed

Suggested Readings

Erro, R, Bhatia, KP, Edwards, MJ, Farmer, SF, Cordivari, C. Clinical diagnosis of propriospinal myoclonus is unreliable: an electrophysiologic study. Mov Disord. 2013;28:1868–73.CrossRefGoogle ScholarPubMed
Erro, R, Edwards, MJ, Bhatia, KP, et al. Psychogenic axial myoclonus: clinical features and long-term outcome. Parkinsonism Relat Disord. 2014;20:596–9.CrossRefGoogle ScholarPubMed
van der Salm, SM, Erro, R, Cordivari, C, et al. Propriospinal myoclonus: clinical reappraisal and review of literature. Neurology. 2014;83:1862–70.CrossRefGoogle ScholarPubMed

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  • Myoclonus
  • Kailash P. Bhatia, Institute of Neurology, University College London, Roberto Erro, Maria Stamelou, University of Athens, Greece
  • Book: Case Studies in Movement Disorders
  • Online publication: 04 July 2017
  • Chapter DOI: https://doi.org/10.1017/9781316145050.053
Available formats
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Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

  • Myoclonus
  • Kailash P. Bhatia, Institute of Neurology, University College London, Roberto Erro, Maria Stamelou, University of Athens, Greece
  • Book: Case Studies in Movement Disorders
  • Online publication: 04 July 2017
  • Chapter DOI: https://doi.org/10.1017/9781316145050.053
Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

  • Myoclonus
  • Kailash P. Bhatia, Institute of Neurology, University College London, Roberto Erro, Maria Stamelou, University of Athens, Greece
  • Book: Case Studies in Movement Disorders
  • Online publication: 04 July 2017
  • Chapter DOI: https://doi.org/10.1017/9781316145050.053
Available formats
×