Annals of Indian Academy of Neurology
CASE REPORT
Year
: 2015  |  Volume : 18  |  Issue : 2  |  Page : 249--251

Fasciculations masquerading as minipolymyoclonus in bulbospinal muscular atrophy


Sushanth Bhat, Wei Ma, Elena Kozochonok, Sudhansu Chokroverty 
 Department of Neurology, JFK Neuroscience Institute, Seton Hall University, Edison, New Jersey, USA

Correspondence Address:
Sushanth Bhat
65 James Street, Edison, New Jersey 08820
USA

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«SQ»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 «DQ»minipolyfasciculations«DQ» may be more reflective of the underlying process causing minipolymyoclonus-like movements in lower motor neuron disorders.


How to cite this article:
Bhat S, Ma W, Kozochonok E, Chokroverty S. Fasciculations masquerading as minipolymyoclonus in bulbospinal muscular atrophy.Ann Indian Acad Neurol 2015;18:249-251


How to cite this URL:
Bhat S, Ma W, Kozochonok E, Chokroverty S. Fasciculations masquerading as minipolymyoclonus in bulbospinal muscular atrophy. Ann Indian Acad Neurol [serial online] 2015 [cited 2019 Jun 25 ];18:249-251
Available from: http://www.annalsofian.org/article.asp?issn=0972-2327;year=2015;volume=18;issue=2;spage=249;epage=251;aulast=Bhat;type=0