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Severe Spinal Injury in Hirayama Disease
Hirayama disease is a rare neurological disorder characterized by an insidious progressive subacute unilateral or bilateral weakness of the hands and forearm muscles leading to a painless amyotrophy. The disease primarily affects young men in the second to third decades of life. It has always been d...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society of Spine Surgery
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4591454/ https://www.ncbi.nlm.nih.gov/pubmed/26435801 http://dx.doi.org/10.4184/asj.2015.9.5.794 |
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author | Quarracino, Cecilia Aguirre, Florencia Rugilo, Carlos A. Negri, Luciana De Villa, Andrés M. |
author_facet | Quarracino, Cecilia Aguirre, Florencia Rugilo, Carlos A. Negri, Luciana De Villa, Andrés M. |
author_sort | Quarracino, Cecilia |
collection | PubMed |
description | Hirayama disease is a rare neurological disorder characterized by an insidious progressive subacute unilateral or bilateral weakness of the hands and forearm muscles leading to a painless amyotrophy. The disease primarily affects young men in the second to third decades of life. It has always been described as a second motor neuron disease, thus sparing the pyramidal and sensitive pathways. It usually has a slow progression course of 3 to 5 years followed by stabilization. Since its initial description by Keyzo Hirayama in 1959, most cases have been reported in Asia, particularly Japan and India, although the disease reportedly has worldwide distribution. |
format | Online Article Text |
id | pubmed-4591454 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Korean Society of Spine Surgery |
record_format | MEDLINE/PubMed |
spelling | pubmed-45914542015-10-04 Severe Spinal Injury in Hirayama Disease Quarracino, Cecilia Aguirre, Florencia Rugilo, Carlos A. Negri, Luciana De Villa, Andrés M. Asian Spine J Case Report Hirayama disease is a rare neurological disorder characterized by an insidious progressive subacute unilateral or bilateral weakness of the hands and forearm muscles leading to a painless amyotrophy. The disease primarily affects young men in the second to third decades of life. It has always been described as a second motor neuron disease, thus sparing the pyramidal and sensitive pathways. It usually has a slow progression course of 3 to 5 years followed by stabilization. Since its initial description by Keyzo Hirayama in 1959, most cases have been reported in Asia, particularly Japan and India, although the disease reportedly has worldwide distribution. Korean Society of Spine Surgery 2015-10 2015-09-22 /pmc/articles/PMC4591454/ /pubmed/26435801 http://dx.doi.org/10.4184/asj.2015.9.5.794 Text en Copyright © 2015 by Korean Society of Spine Surgery 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 Quarracino, Cecilia Aguirre, Florencia Rugilo, Carlos A. Negri, Luciana De Villa, Andrés M. Severe Spinal Injury in Hirayama Disease |
title | Severe Spinal Injury in Hirayama Disease |
title_full | Severe Spinal Injury in Hirayama Disease |
title_fullStr | Severe Spinal Injury in Hirayama Disease |
title_full_unstemmed | Severe Spinal Injury in Hirayama Disease |
title_short | Severe Spinal Injury in Hirayama Disease |
title_sort | severe spinal injury in hirayama disease |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4591454/ https://www.ncbi.nlm.nih.gov/pubmed/26435801 http://dx.doi.org/10.4184/asj.2015.9.5.794 |
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