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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...

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Autores principales: Quarracino, Cecilia, Aguirre, Florencia, Rugilo, Carlos A., Negri, Luciana De, Villa, Andrés M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Spine Surgery 2015
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.
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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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