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Auricular Myoclonus: A Case Report and Literature Review

Auricular myoclonus is an extremely rare disorder that manifests as involuntary semi-rhythmic movements of the auricle. We report the case of a 15-year-old female who presented to our outpatient clinics with bilateral spontaneous, uncontrolled movements of the auricles (auricular myoclonus) that are...

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Autores principales: E. Jabbour, Christopher, A. Sawaya, Raja, M. Zaytoun, George
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Academy of Otology and Neurotology and the Politzer Society 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8975402/
https://www.ncbi.nlm.nih.gov/pubmed/35177400
http://dx.doi.org/10.5152/iao.2021.21064
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author E. Jabbour, Christopher
A. Sawaya, Raja
M. Zaytoun, George
author_facet E. Jabbour, Christopher
A. Sawaya, Raja
M. Zaytoun, George
author_sort E. Jabbour, Christopher
collection PubMed
description Auricular myoclonus is an extremely rare disorder that manifests as involuntary semi-rhythmic movements of the auricle. We report the case of a 15-year-old female who presented to our outpatient clinics with bilateral spontaneous, uncontrolled movements of the auricles (auricular myoclonus) that are only briefly suppressible by some facial movements and completely disappear during sleep. Needle electromyography revealed baseline tonic motor unit activity with bursts of higher motor units amplitude in the posterior and superior auricularis muscles. Her symptoms improved with pregabalin intake, however, with incomplete resolution. This paper will review previously reported cases, as well as the different treatment modalities that have been used.
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spelling pubmed-89754022022-04-14 Auricular Myoclonus: A Case Report and Literature Review E. Jabbour, Christopher A. Sawaya, Raja M. Zaytoun, George J Int Adv Otol Case Report Auricular myoclonus is an extremely rare disorder that manifests as involuntary semi-rhythmic movements of the auricle. We report the case of a 15-year-old female who presented to our outpatient clinics with bilateral spontaneous, uncontrolled movements of the auricles (auricular myoclonus) that are only briefly suppressible by some facial movements and completely disappear during sleep. Needle electromyography revealed baseline tonic motor unit activity with bursts of higher motor units amplitude in the posterior and superior auricularis muscles. Her symptoms improved with pregabalin intake, however, with incomplete resolution. This paper will review previously reported cases, as well as the different treatment modalities that have been used. European Academy of Otology and Neurotology and the Politzer Society 2021-11-01 /pmc/articles/PMC8975402/ /pubmed/35177400 http://dx.doi.org/10.5152/iao.2021.21064 Text en 2021 authors https://creativecommons.org/licenses/by-nc/4.0/ Content of this journal is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. (https://creativecommons.org/licenses/by-nc/4.0/)
spellingShingle Case Report
E. Jabbour, Christopher
A. Sawaya, Raja
M. Zaytoun, George
Auricular Myoclonus: A Case Report and Literature Review
title Auricular Myoclonus: A Case Report and Literature Review
title_full Auricular Myoclonus: A Case Report and Literature Review
title_fullStr Auricular Myoclonus: A Case Report and Literature Review
title_full_unstemmed Auricular Myoclonus: A Case Report and Literature Review
title_short Auricular Myoclonus: A Case Report and Literature Review
title_sort auricular myoclonus: a case report and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8975402/
https://www.ncbi.nlm.nih.gov/pubmed/35177400
http://dx.doi.org/10.5152/iao.2021.21064
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