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A case of idiopathic isolated hypoglossal nerve palsy in a Korean child

Hypoglossal nerve palsy (HNP) is an uncommon neurological abnormality that can provoke characteristic clinical signs, including unilateral atrophy of the tongue musculature. We present the case of a healthy 11-year-old Korean male who was admitted to the outpatient department of our institution with...

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Autores principales: Yoon, Ji Hoi, Cho, Kyung Lae, Lee, Hae Jung, Choi, Seo Hui, Lee, Kyung Yul, Kim, Sung Koo, Lee, Jun Hwa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Pediatric Society 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3274659/
https://www.ncbi.nlm.nih.gov/pubmed/22323909
http://dx.doi.org/10.3345/kjp.2011.54.12.515
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author Yoon, Ji Hoi
Cho, Kyung Lae
Lee, Hae Jung
Choi, Seo Hui
Lee, Kyung Yul
Kim, Sung Koo
Lee, Jun Hwa
author_facet Yoon, Ji Hoi
Cho, Kyung Lae
Lee, Hae Jung
Choi, Seo Hui
Lee, Kyung Yul
Kim, Sung Koo
Lee, Jun Hwa
author_sort Yoon, Ji Hoi
collection PubMed
description Hypoglossal nerve palsy (HNP) is an uncommon neurological abnormality that can provoke characteristic clinical signs, including unilateral atrophy of the tongue musculature. We present the case of a healthy 11-year-old Korean male who was admitted to the outpatient department of our institution with acute onset dysarthria, tongue fasciculations, and right-sided tongue weakness upon awakening. His evaluation included a virology work-up, neck magnetic resonance imaging (MRI), brain MRI, and otorhinolaryngological physical examination; all tests were normal and showed no evidence of inflammation. Fifteen days after the onset of symptoms, the patient recovered completely. Herein, we report a case of idiopathic isolated HNP in a Korean male.
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spelling pubmed-32746592012-02-09 A case of idiopathic isolated hypoglossal nerve palsy in a Korean child Yoon, Ji Hoi Cho, Kyung Lae Lee, Hae Jung Choi, Seo Hui Lee, Kyung Yul Kim, Sung Koo Lee, Jun Hwa Korean J Pediatr Case Report Hypoglossal nerve palsy (HNP) is an uncommon neurological abnormality that can provoke characteristic clinical signs, including unilateral atrophy of the tongue musculature. We present the case of a healthy 11-year-old Korean male who was admitted to the outpatient department of our institution with acute onset dysarthria, tongue fasciculations, and right-sided tongue weakness upon awakening. His evaluation included a virology work-up, neck magnetic resonance imaging (MRI), brain MRI, and otorhinolaryngological physical examination; all tests were normal and showed no evidence of inflammation. Fifteen days after the onset of symptoms, the patient recovered completely. Herein, we report a case of idiopathic isolated HNP in a Korean male. The Korean Pediatric Society 2011-12 2011-12-31 /pmc/articles/PMC3274659/ /pubmed/22323909 http://dx.doi.org/10.3345/kjp.2011.54.12.515 Text en Copyright © 2011 by The Korean Pediatric Society http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Yoon, Ji Hoi
Cho, Kyung Lae
Lee, Hae Jung
Choi, Seo Hui
Lee, Kyung Yul
Kim, Sung Koo
Lee, Jun Hwa
A case of idiopathic isolated hypoglossal nerve palsy in a Korean child
title A case of idiopathic isolated hypoglossal nerve palsy in a Korean child
title_full A case of idiopathic isolated hypoglossal nerve palsy in a Korean child
title_fullStr A case of idiopathic isolated hypoglossal nerve palsy in a Korean child
title_full_unstemmed A case of idiopathic isolated hypoglossal nerve palsy in a Korean child
title_short A case of idiopathic isolated hypoglossal nerve palsy in a Korean child
title_sort case of idiopathic isolated hypoglossal nerve palsy in a korean child
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3274659/
https://www.ncbi.nlm.nih.gov/pubmed/22323909
http://dx.doi.org/10.3345/kjp.2011.54.12.515
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