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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Main Authors: Cecilia Quarracino, Florencia Aguirre, Carlos A. Rugilo, Luciana De Negri, Andrés M. Villa
Format: Article
Language:English
Published: Korean Spine Society 2015-10-01
Series:Asian Spine Journal
Subjects:
Online Access:http://www.asianspinejournal.org/upload/pdf/asj-9-794.pdf
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author Cecilia Quarracino
Florencia Aguirre
Carlos A. Rugilo
Luciana De Negri
Andrés M. Villa
author_facet Cecilia Quarracino
Florencia Aguirre
Carlos A. Rugilo
Luciana De Negri
Andrés M. Villa
author_sort Cecilia Quarracino
collection DOAJ
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 doaj.art-6cc9a6f0351547c1ab2649ab60eb586a2022-12-21T18:59:13ZengKorean Spine SocietyAsian Spine Journal1976-19021976-78462015-10-019579479710.4184/asj.2015.9.5.794860Severe Spinal Injury in Hirayama DiseaseCecilia Quarracino0Florencia Aguirre1Carlos A. Rugilo2Luciana De Negri3Andrés M. Villa4Neuroimmunology and Electrophysiology Section, Neurology Department, Ramos Mejía Hospital, Buenos Aires University School of Medicine, Buenos Aires, Argentina.Neuroimmunology and Electrophysiology Section, Neurology Department, Ramos Mejía Hospital, Buenos Aires University School of Medicine, Buenos Aires, Argentina.Neuroradiology Section, British Hospital of Buenos Aires, Buenos Aires, Argentina.Neuroimmunology and Electrophysiology Section, Neurology Department, Ramos Mejía Hospital, Buenos Aires University School of Medicine, Buenos Aires, Argentina.Neuroimmunology and Electrophysiology Section, Neurology Department, Ramos Mejía Hospital, Buenos Aires University School of Medicine, Buenos Aires, Argentina.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.http://www.asianspinejournal.org/upload/pdf/asj-9-794.pdfHirayama diseaseOblique amyotrophyHand atrophySegmental spinal atrophyDynamic myelopathy
spellingShingle Cecilia Quarracino
Florencia Aguirre
Carlos A. Rugilo
Luciana De Negri
Andrés M. Villa
Severe Spinal Injury in Hirayama Disease
Asian Spine Journal
Hirayama disease
Oblique amyotrophy
Hand atrophy
Segmental spinal atrophy
Dynamic myelopathy
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 Hirayama disease
Oblique amyotrophy
Hand atrophy
Segmental spinal atrophy
Dynamic myelopathy
url http://www.asianspinejournal.org/upload/pdf/asj-9-794.pdf
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