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36 - Myoclonus

from PART III - DISORDERS OF MOTOR CONTROL

Published online by Cambridge University Press:  05 August 2016

Peter Brown
Affiliation:
Sobell Department of Motor Neuroscience, Institute of Neurology
Arthur K. Asbury
Affiliation:
University of Pennsylvania School of Medicine
Guy M. McKhann
Affiliation:
The Johns Hopkins University School of Medicine
W. Ian McDonald
Affiliation:
University College London
Peter J. Goadsby
Affiliation:
University College London
Justin C. McArthur
Affiliation:
The Johns Hopkins University School of Medicine
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Summary

Myoclonus is defined as shock-like involuntary movements. Most often these are due to brief bursts of muscle activity, resulting in positive myoclonus. Jerks, however, may also result from sudden short inhibitions of ongoing tonic muscle activity, termed negative myoclonus or asterixis. Myoclonus may be physiological, such as hiccups, or due to a variety of hereditary or acquired conditions. In particular, it may be seen in primary generalized epilepsy, but as this syndrome is dominated by epilepsy rather than myoclonus, it will not be considered further here.

Clinical overview of physiologically based classification

Although etiological classifications have not proven very useful in predicting the response to drugs, electrophysiological investigations have been able to distinguish several different pathophysiological mechanisms with therapeutic implications. To a large degree, the pathophysiological type of myoclonus can be suspected on clinical grounds. The most useful clinical distinction is between generalized, multifocal and focal/segmental jerks. Generalized myoclonus involves the majority of the body in a synchronous jerk. It may spare the face and be predominantly axial, as in propriospinal myoclonus, or include the face, as in brainstem myoclonus. The latter may only consist of reflex jerks, as in exaggerated startle/hyperekplexia, or may also involve prominent spontaneous jerks as in brainstem reticular reflex myoclonus. A useful confirmatory sign of a brainstem origin is the presence of jerks in response to auditory stimulation, particularly unexpected sounds. Multifocal myoclonus involves different parts of the body at different times. There may also be the occasional generalized jerk, but the clinical picture is dominated by multifocal jerks. Such patients may be divided into those in whom the distal limbs are especially involved, and are likely to have cortical myoclonus, and those in whom the jerks are most noticeable proximally, particularly round the shoulders. These are likely to have essential myoclonus. Helpful confirmatory signs of cortical and essential myoclonus are an exacerbation of jerking upon voluntary action and the presence of dystonic posturing, respectively. Focal/segmental jerks are the most obscure as they may arise at virtually any level of the nervous system, including the spinal cord.

Clinical suspicion of particular pathophysiological types of myoclonus can be supported by simple investigation.

Type
Chapter
Information
Diseases of the Nervous System
Clinical Neuroscience and Therapeutic Principles
, pp. 523 - 531
Publisher: Cambridge University Press
Print publication year: 2002

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  • Myoclonus
    • By Peter Brown, Sobell Department of Motor Neuroscience, Institute of Neurology
  • Edited by Arthur K. Asbury, University of Pennsylvania School of Medicine, Guy M. McKhann, The Johns Hopkins University School of Medicine, W. Ian McDonald, University College London, Peter J. Goadsby, University College London, Justin C. McArthur, The Johns Hopkins University School of Medicine
  • Book: Diseases of the Nervous System
  • Online publication: 05 August 2016
  • Chapter DOI: https://doi.org/10.1017/CBO9781316134993.037
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  • Myoclonus
    • By Peter Brown, Sobell Department of Motor Neuroscience, Institute of Neurology
  • Edited by Arthur K. Asbury, University of Pennsylvania School of Medicine, Guy M. McKhann, The Johns Hopkins University School of Medicine, W. Ian McDonald, University College London, Peter J. Goadsby, University College London, Justin C. McArthur, The Johns Hopkins University School of Medicine
  • Book: Diseases of the Nervous System
  • Online publication: 05 August 2016
  • Chapter DOI: https://doi.org/10.1017/CBO9781316134993.037
Available formats
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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
    • By Peter Brown, Sobell Department of Motor Neuroscience, Institute of Neurology
  • Edited by Arthur K. Asbury, University of Pennsylvania School of Medicine, Guy M. McKhann, The Johns Hopkins University School of Medicine, W. Ian McDonald, University College London, Peter J. Goadsby, University College London, Justin C. McArthur, The Johns Hopkins University School of Medicine
  • Book: Diseases of the Nervous System
  • Online publication: 05 August 2016
  • Chapter DOI: https://doi.org/10.1017/CBO9781316134993.037
Available formats
×