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Sporadic hyperekplexia due to self-limiting brainstem encephalopathy

Hyperekplexia is a rare movement disorder characterized by pathologically exaggerated response to unexpected stimuli. It is differentiated from the normal startle reflex by its lower threshold, higher intensity, and resistance to habituation. Many of the acquired hyperekplexias result from brainstem...

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Detalles Bibliográficos
Autores principales: Yilmaz, Dilek, Cengiz, Bülent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5640391/
https://www.ncbi.nlm.nih.gov/pubmed/29062233
http://dx.doi.org/10.2147/NDT.S142609
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author Yilmaz, Dilek
Cengiz, Bülent
author_facet Yilmaz, Dilek
Cengiz, Bülent
author_sort Yilmaz, Dilek
collection PubMed
description Hyperekplexia is a rare movement disorder characterized by pathologically exaggerated response to unexpected stimuli. It is differentiated from the normal startle reflex by its lower threshold, higher intensity, and resistance to habituation. Many of the acquired hyperekplexias result from brainstem involvement such as encephalitis, infarct, hemorrhage, pontocerebellar hypoplasia and medullary compression. This case report depicts a rare manifestation of hyperekplexia. The unusual aspect of this case was the vocalization that was reproduced in response to startling stimuli. Startle induced vocalization is not a part of the classical hyperekplexia description. When faced with a patient with pathologically exaggerated response to unexpected stimuli, the physician should consider this rare condition in the differential diagnosis, and also keep in mind that the disease may present with features different from those listed in the textbooks.
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spelling pubmed-56403912017-10-23 Sporadic hyperekplexia due to self-limiting brainstem encephalopathy Yilmaz, Dilek Cengiz, Bülent Neuropsychiatr Dis Treat Case Report Hyperekplexia is a rare movement disorder characterized by pathologically exaggerated response to unexpected stimuli. It is differentiated from the normal startle reflex by its lower threshold, higher intensity, and resistance to habituation. Many of the acquired hyperekplexias result from brainstem involvement such as encephalitis, infarct, hemorrhage, pontocerebellar hypoplasia and medullary compression. This case report depicts a rare manifestation of hyperekplexia. The unusual aspect of this case was the vocalization that was reproduced in response to startling stimuli. Startle induced vocalization is not a part of the classical hyperekplexia description. When faced with a patient with pathologically exaggerated response to unexpected stimuli, the physician should consider this rare condition in the differential diagnosis, and also keep in mind that the disease may present with features different from those listed in the textbooks. Dove Medical Press 2017-10-09 /pmc/articles/PMC5640391/ /pubmed/29062233 http://dx.doi.org/10.2147/NDT.S142609 Text en © 2017 Yilmaz and Cengiz. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Case Report
Yilmaz, Dilek
Cengiz, Bülent
Sporadic hyperekplexia due to self-limiting brainstem encephalopathy
title Sporadic hyperekplexia due to self-limiting brainstem encephalopathy
title_full Sporadic hyperekplexia due to self-limiting brainstem encephalopathy
title_fullStr Sporadic hyperekplexia due to self-limiting brainstem encephalopathy
title_full_unstemmed Sporadic hyperekplexia due to self-limiting brainstem encephalopathy
title_short Sporadic hyperekplexia due to self-limiting brainstem encephalopathy
title_sort sporadic hyperekplexia due to self-limiting brainstem encephalopathy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5640391/
https://www.ncbi.nlm.nih.gov/pubmed/29062233
http://dx.doi.org/10.2147/NDT.S142609
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