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Correlations of clinical, neuroimaging, and electrophysiological features in Hirayama disease
Hirayama disease (HD) is characterized by development of asymmetric forearm muscle atrophy during adolescence with or without focal cervical spinal cord atrophy. The purpose of this study is to assess the correlation of clinical symptoms, disease progression, and electrophysiological findings with c...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4956817/ https://www.ncbi.nlm.nih.gov/pubmed/27428223 http://dx.doi.org/10.1097/MD.0000000000004210 |
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author | Liao, Ming-Feng Chang, Hong-Shiu Chang, Kuo-Hsuan Ro, Long-Sun Chu, Chun-Che Kuo, Hung-Chou Lyu, Rong-Kuo |
author_facet | Liao, Ming-Feng Chang, Hong-Shiu Chang, Kuo-Hsuan Ro, Long-Sun Chu, Chun-Che Kuo, Hung-Chou Lyu, Rong-Kuo |
author_sort | Liao, Ming-Feng |
collection | PubMed |
description | Hirayama disease (HD) is characterized by development of asymmetric forearm muscle atrophy during adolescence with or without focal cervical spinal cord atrophy. The purpose of this study is to assess the correlation of clinical symptoms, disease progression, and electrophysiological findings with cervical spine magnetic resonance imaging (MRI) findings. The medical records, cervical spine MRIs, and electrophysiological findings of 44 HD patients were retrospectively reviewed and analyzed. Denervation changes in any single C5 to C7 root-innervated muscle (deltoid, biceps, triceps, or extensor digitorum communis) occurred more frequently in the 25 patients with cord atrophy than the 19 patients without cord atrophy (88% vs 53%, P = 0.02). Onset age, duration of disease progression, neurological examinations, nerve conduction study, and electromyographic findings from individual muscles were similar between patient groups. Compared with HD patients without cord atrophy, HD patients with cord atrophy experience a more severe denervation change in C5 to C7 root-innervated muscles. |
format | Online Article Text |
id | pubmed-4956817 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-49568172016-08-02 Correlations of clinical, neuroimaging, and electrophysiological features in Hirayama disease Liao, Ming-Feng Chang, Hong-Shiu Chang, Kuo-Hsuan Ro, Long-Sun Chu, Chun-Che Kuo, Hung-Chou Lyu, Rong-Kuo Medicine (Baltimore) 5300 Hirayama disease (HD) is characterized by development of asymmetric forearm muscle atrophy during adolescence with or without focal cervical spinal cord atrophy. The purpose of this study is to assess the correlation of clinical symptoms, disease progression, and electrophysiological findings with cervical spine magnetic resonance imaging (MRI) findings. The medical records, cervical spine MRIs, and electrophysiological findings of 44 HD patients were retrospectively reviewed and analyzed. Denervation changes in any single C5 to C7 root-innervated muscle (deltoid, biceps, triceps, or extensor digitorum communis) occurred more frequently in the 25 patients with cord atrophy than the 19 patients without cord atrophy (88% vs 53%, P = 0.02). Onset age, duration of disease progression, neurological examinations, nerve conduction study, and electromyographic findings from individual muscles were similar between patient groups. Compared with HD patients without cord atrophy, HD patients with cord atrophy experience a more severe denervation change in C5 to C7 root-innervated muscles. Wolters Kluwer Health 2016-07-18 /pmc/articles/PMC4956817/ /pubmed/27428223 http://dx.doi.org/10.1097/MD.0000000000004210 Text en Copyright © 2016 the Author(s). Published by Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0, where it is permissible to download, share and reproduce the work in any medium, provided it is properly cited. The work cannot be changed in any way or used commercially. http://creativecommons.org/licenses/by-nc-nd/4.0 |
spellingShingle | 5300 Liao, Ming-Feng Chang, Hong-Shiu Chang, Kuo-Hsuan Ro, Long-Sun Chu, Chun-Che Kuo, Hung-Chou Lyu, Rong-Kuo Correlations of clinical, neuroimaging, and electrophysiological features in Hirayama disease |
title | Correlations of clinical, neuroimaging, and electrophysiological features in Hirayama disease |
title_full | Correlations of clinical, neuroimaging, and electrophysiological features in Hirayama disease |
title_fullStr | Correlations of clinical, neuroimaging, and electrophysiological features in Hirayama disease |
title_full_unstemmed | Correlations of clinical, neuroimaging, and electrophysiological features in Hirayama disease |
title_short | Correlations of clinical, neuroimaging, and electrophysiological features in Hirayama disease |
title_sort | correlations of clinical, neuroimaging, and electrophysiological features in hirayama disease |
topic | 5300 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4956817/ https://www.ncbi.nlm.nih.gov/pubmed/27428223 http://dx.doi.org/10.1097/MD.0000000000004210 |
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