Literature DB >> 17415799

Persisting hyperekplexia after idiopathic, self-limiting brainstem encephalopathy.

Bart P C van de Warrenburg1, Carla Cordivari, Peter Brown, Kailash P Bhatia.   

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. (c) 2007 Movement Disorder Society.

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Year:  2007        PMID: 17415799     DOI: 10.1002/mds.21411

Source DB:  PubMed          Journal:  Mov Disord        ISSN: 0885-3185            Impact factor:   10.338


  4 in total

1.  Treatment of Complex Regional Pain Syndrome (CRPS) using low dose naltrexone (LDN).

Authors:  Pradeep Chopra; Mark S Cooper
Journal:  J Neuroimmune Pharmacol       Date:  2013-04-02       Impact factor: 4.147

2.  Sporadic hyperekplexia due to self-limiting brainstem encephalopathy.

Authors:  Dilek Yilmaz; Bülent Cengiz
Journal:  Neuropsychiatr Dis Treat       Date:  2017-10-09       Impact factor: 2.570

3.  Principles of Electrophysiological Assessments for Movement Disorders.

Authors:  Kai-Hsiang Stanley Chen; Robert Chen
Journal:  J Mov Disord       Date:  2020-01-31

4.  An Unusual Startling.

Authors:  Ibrahim Aliyu; Zainab Ibrahim
Journal:  Indian J Psychol Med       Date:  2015 Oct-Dec
  4 in total

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