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Hirayama Disease with Proximal Involvement

Hirayama disease is a slowly progressing benign motor neuron disease that affects the distal upper limb. A 29-year-old man visited the hospital with a 1-year history of weakened left proximal upper limb. He was diagnosed with Hirayama disease 9 years ago, while there was no further progression of th...

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Detalles Bibliográficos
Autores principales: Kim, Jinil, Kim, Yuntae, Kim, Sooa, Oh, Kiyoung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Academy of Medical Sciences 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4999413/
https://www.ncbi.nlm.nih.gov/pubmed/27550499
http://dx.doi.org/10.3346/jkms.2016.31.10.1664
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author Kim, Jinil
Kim, Yuntae
Kim, Sooa
Oh, Kiyoung
author_facet Kim, Jinil
Kim, Yuntae
Kim, Sooa
Oh, Kiyoung
author_sort Kim, Jinil
collection PubMed
description Hirayama disease is a slowly progressing benign motor neuron disease that affects the distal upper limb. A 29-year-old man visited the hospital with a 1-year history of weakened left proximal upper limb. He was diagnosed with Hirayama disease 9 years ago, while there was no further progression of the muscle weakness afterward. Atrophy and weakness was detected in proximal upper limb muscles. Magnetic resonance imaging and somatosensory evoked potentials were normal. Needle electromyography showed abnormal findings in proximal upper limb muscles. Our patient had Hirayama disease involving the proximal portion through secondary progression. Clinical manifestation and accurate electromyography may be useful for diagnosis. Rare cases with progression patterns as described here are helpful and have clinical meaning for clinicians.
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spelling pubmed-49994132016-10-01 Hirayama Disease with Proximal Involvement Kim, Jinil Kim, Yuntae Kim, Sooa Oh, Kiyoung J Korean Med Sci Case Report Hirayama disease is a slowly progressing benign motor neuron disease that affects the distal upper limb. A 29-year-old man visited the hospital with a 1-year history of weakened left proximal upper limb. He was diagnosed with Hirayama disease 9 years ago, while there was no further progression of the muscle weakness afterward. Atrophy and weakness was detected in proximal upper limb muscles. Magnetic resonance imaging and somatosensory evoked potentials were normal. Needle electromyography showed abnormal findings in proximal upper limb muscles. Our patient had Hirayama disease involving the proximal portion through secondary progression. Clinical manifestation and accurate electromyography may be useful for diagnosis. Rare cases with progression patterns as described here are helpful and have clinical meaning for clinicians. The Korean Academy of Medical Sciences 2016-10 2016-07-21 /pmc/articles/PMC4999413/ /pubmed/27550499 http://dx.doi.org/10.3346/jkms.2016.31.10.1664 Text en © 2016 The Korean Academy of Medical Sciences. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Kim, Jinil
Kim, Yuntae
Kim, Sooa
Oh, Kiyoung
Hirayama Disease with Proximal Involvement
title Hirayama Disease with Proximal Involvement
title_full Hirayama Disease with Proximal Involvement
title_fullStr Hirayama Disease with Proximal Involvement
title_full_unstemmed Hirayama Disease with Proximal Involvement
title_short Hirayama Disease with Proximal Involvement
title_sort hirayama disease with proximal involvement
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4999413/
https://www.ncbi.nlm.nih.gov/pubmed/27550499
http://dx.doi.org/10.3346/jkms.2016.31.10.1664
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