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Paroxysmal movement disorders.

Authors :
Waln O
Jankovic J
Source :
Neurologic clinics [Neurol Clin] 2015 Feb; Vol. 33 (1), pp. 137-52.
Publication Year :
2015

Abstract

Paroxysmal dyskinesias represent a group of episodic abnormal involuntary movements manifested by recurrent attacks of dystonia, chorea, athetosis, or a combination of these disorders. Paroxysmal kinesigenic dyskinesia, paroxysmal nonkinesigenic dyskinesia, paroxysmal exertion-induced dyskinesia, and paroxysmal hypnogenic dyskinesia are distinguished clinically by precipitating factors, duration and frequency of attacks, and response to medication. Primary paroxysmal dyskinesias are usually autosomal dominant genetic conditions. Secondary paroxysmal dyskinesias can be the symptoms of different neurologic and medical disorders. This review summarizes the updates on etiology, pathophysiology, genetics, clinical presentation, differential diagnosis, and treatment of paroxysmal dyskinesias and other episodic movement disorders.<br /> (Copyright © 2015 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1557-9875
Volume :
33
Issue :
1
Database :
MEDLINE
Journal :
Neurologic clinics
Publication Type :
Academic Journal
Accession number :
25432727
Full Text :
https://doi.org/10.1016/j.ncl.2014.09.014