Persisting hyperekplexia after idiopathic, self‐limiting brainstem encephalopathy
Identifieur interne : 001785 ( Istex/Checkpoint ); précédent : 001784; suivant : 001786Persisting hyperekplexia after idiopathic, self‐limiting brainstem encephalopathy
Auteurs : Bart P. C. Van De Warrenburg [Royaume-Uni, Pays-Bas] ; Carla Cordivari [Royaume-Uni] ; Peter Brown [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni]Source :
- Movement Disorders [ 0885-3185 ] ; 2007-05-15.
English descriptors
Abstract
Symptomatic hyperekplexia is a relatively rare entity, but has been documented in various, mostly brainstem diseases. We report the clinical and neurophysiologic vignette of a patient with a self‐limiting, possibly inflammatory brainstem encephalopathy. Trismus was the presenting feature, but she later developed hyperekplexia. Although most brainstem features resolved spontaneously, the hyperekplexia has persisted. © 2007 Movement Disorder Society
Url:
DOI: 10.1002/mds.21411
Affiliations:
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<front><div type="abstract" xml:lang="en">Symptomatic hyperekplexia is a relatively rare entity, but has been documented in various, mostly brainstem diseases. We report the clinical and neurophysiologic vignette of a patient with a self‐limiting, possibly inflammatory brainstem encephalopathy. Trismus was the presenting feature, but she later developed hyperekplexia. Although most brainstem features resolved spontaneously, the hyperekplexia has persisted. © 2007 Movement Disorder Society</div>
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