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Fasciculations masquerading as minipolymyoclonus in bulbospinal muscular atrophy
Minipolymyoclonus has been described in both anterior horn cell disorders and central nervous system degenerative conditions. While its etiology remains unclear and speculative, a central generator has been previously proposed. We describe a case of bulbospinal muscular atrophy (Kennedy's disea...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4445210/ https://www.ncbi.nlm.nih.gov/pubmed/26019432 http://dx.doi.org/10.4103/0972-2327.150624 |
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author | Bhat, Sushanth Ma, Wei Kozochonok, Elena Chokroverty, Sudhansu |
author_facet | Bhat, Sushanth Ma, Wei Kozochonok, Elena Chokroverty, Sudhansu |
author_sort | Bhat, Sushanth |
collection | PubMed |
description | Minipolymyoclonus has been described in both anterior horn cell disorders and central nervous system degenerative conditions. While its etiology remains unclear and speculative, a central generator has been previously proposed. We describe a case of bulbospinal muscular atrophy (Kennedy's disease), where minipolymyoclonus-like movements corresponded to fasciculations in neurophysiological studies. Our novel finding suggests that the etiologies of minipolymyoclonus in central and peripheral nervous system disorders are distinct, despite outward clinical similarity. The term “minipolyfasciculations” may be more reflective of the underlying process causing minipolymyoclonus-like movements in lower motor neuron disorders. |
format | Online Article Text |
id | pubmed-4445210 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-44452102015-05-27 Fasciculations masquerading as minipolymyoclonus in bulbospinal muscular atrophy Bhat, Sushanth Ma, Wei Kozochonok, Elena Chokroverty, Sudhansu Ann Indian Acad Neurol Case Report Minipolymyoclonus has been described in both anterior horn cell disorders and central nervous system degenerative conditions. While its etiology remains unclear and speculative, a central generator has been previously proposed. We describe a case of bulbospinal muscular atrophy (Kennedy's disease), where minipolymyoclonus-like movements corresponded to fasciculations in neurophysiological studies. Our novel finding suggests that the etiologies of minipolymyoclonus in central and peripheral nervous system disorders are distinct, despite outward clinical similarity. The term “minipolyfasciculations” may be more reflective of the underlying process causing minipolymyoclonus-like movements in lower motor neuron disorders. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4445210/ /pubmed/26019432 http://dx.doi.org/10.4103/0972-2327.150624 Text en Copyright: © Annals of Indian Academy of Neurology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Bhat, Sushanth Ma, Wei Kozochonok, Elena Chokroverty, Sudhansu Fasciculations masquerading as minipolymyoclonus in bulbospinal muscular atrophy |
title | Fasciculations masquerading as minipolymyoclonus in bulbospinal muscular atrophy |
title_full | Fasciculations masquerading as minipolymyoclonus in bulbospinal muscular atrophy |
title_fullStr | Fasciculations masquerading as minipolymyoclonus in bulbospinal muscular atrophy |
title_full_unstemmed | Fasciculations masquerading as minipolymyoclonus in bulbospinal muscular atrophy |
title_short | Fasciculations masquerading as minipolymyoclonus in bulbospinal muscular atrophy |
title_sort | fasciculations masquerading as minipolymyoclonus in bulbospinal muscular atrophy |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4445210/ https://www.ncbi.nlm.nih.gov/pubmed/26019432 http://dx.doi.org/10.4103/0972-2327.150624 |
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