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Hirayama disease

A 17-year-old male, who gave up his favorite sport cricket and started playing football, presented with one-year history of slowly progressive atrophic weakness of forearms and hands. Neurological examination showed weak and wasted arms, forearms and hand but no evidence of pyramidal tract, spinotha...

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Detalles Bibliográficos
Autores principales: Tayade, Atul T, Kale, Sushilkumar K, Pandey, Arvind, Kalantri, Shriprakash
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3137836/
https://www.ncbi.nlm.nih.gov/pubmed/21799622
http://dx.doi.org/10.4103/0976-3147.63105
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author Tayade, Atul T
Kale, Sushilkumar K
Pandey, Arvind
Kalantri, Shriprakash
author_facet Tayade, Atul T
Kale, Sushilkumar K
Pandey, Arvind
Kalantri, Shriprakash
author_sort Tayade, Atul T
collection PubMed
description A 17-year-old male, who gave up his favorite sport cricket and started playing football, presented with one-year history of slowly progressive atrophic weakness of forearms and hands. Neurological examination showed weak and wasted arms, forearms and hand but no evidence of pyramidal tract, spinothalmic tract and posterior column lesions. Plain cervical spine radiographs showed no abnormal findings. Cervical magnetic resonance imaging (MRI) showed asymmetric cord atrophy; images obtained with neck flexed showed the anterior shifting of the posterior wall of the lower cervical dural sac resulting in cord compression. These findings suggest Hirayama disease, a kind of cervical myelopathy related to the flexion movements of the neck.
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spelling pubmed-31378362011-07-28 Hirayama disease Tayade, Atul T Kale, Sushilkumar K Pandey, Arvind Kalantri, Shriprakash J Neurosci Rural Pract Case Report A 17-year-old male, who gave up his favorite sport cricket and started playing football, presented with one-year history of slowly progressive atrophic weakness of forearms and hands. Neurological examination showed weak and wasted arms, forearms and hand but no evidence of pyramidal tract, spinothalmic tract and posterior column lesions. Plain cervical spine radiographs showed no abnormal findings. Cervical magnetic resonance imaging (MRI) showed asymmetric cord atrophy; images obtained with neck flexed showed the anterior shifting of the posterior wall of the lower cervical dural sac resulting in cord compression. These findings suggest Hirayama disease, a kind of cervical myelopathy related to the flexion movements of the neck. Medknow Publications 2010 /pmc/articles/PMC3137836/ /pubmed/21799622 http://dx.doi.org/10.4103/0976-3147.63105 Text en © Journal of Neurosciences in Rural Practice http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Tayade, Atul T
Kale, Sushilkumar K
Pandey, Arvind
Kalantri, Shriprakash
Hirayama disease
title Hirayama disease
title_full Hirayama disease
title_fullStr Hirayama disease
title_full_unstemmed Hirayama disease
title_short Hirayama disease
title_sort hirayama disease
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3137836/
https://www.ncbi.nlm.nih.gov/pubmed/21799622
http://dx.doi.org/10.4103/0976-3147.63105
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