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Hirayama's Disease: A Rare Clinical Variant of Amyotrophic Lateral Sclerosis

Hirayama's disease is a rare clinical variant of amyotrophic lateral sclerosis where distal muscles are involved more compared to proximal muscles and vice-versa occurs only in 10% cases and so it is differentiated from O’Sullivan McLeod syndrome which involves only small muscles of single limb...

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Autores principales: Aundhakar, Swati C., Mahajan, Sanket K., Chhapra, Daanish A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5549545/
https://www.ncbi.nlm.nih.gov/pubmed/28828346
http://dx.doi.org/10.4103/2277-9175.211797
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author Aundhakar, Swati C.
Mahajan, Sanket K.
Chhapra, Daanish A.
author_facet Aundhakar, Swati C.
Mahajan, Sanket K.
Chhapra, Daanish A.
author_sort Aundhakar, Swati C.
collection PubMed
description Hirayama's disease is a rare clinical variant of amyotrophic lateral sclerosis where distal muscles are involved more compared to proximal muscles and vice-versa occurs only in 10% cases and so it is differentiated from O’Sullivan McLeod syndrome which involves only small muscles of single limb. Here, we present a case of Hirayama's disease where disease achieved a plateau after 3 years with no further progression. His electrophysiological studies, and clinical picture, and magnetic resonance imaging findings were consistent with a diagnosis of Hirayama's disease.
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spelling pubmed-55495452017-08-21 Hirayama's Disease: A Rare Clinical Variant of Amyotrophic Lateral Sclerosis Aundhakar, Swati C. Mahajan, Sanket K. Chhapra, Daanish A. Adv Biomed Res Case Report Hirayama's disease is a rare clinical variant of amyotrophic lateral sclerosis where distal muscles are involved more compared to proximal muscles and vice-versa occurs only in 10% cases and so it is differentiated from O’Sullivan McLeod syndrome which involves only small muscles of single limb. Here, we present a case of Hirayama's disease where disease achieved a plateau after 3 years with no further progression. His electrophysiological studies, and clinical picture, and magnetic resonance imaging findings were consistent with a diagnosis of Hirayama's disease. Medknow Publications & Media Pvt Ltd 2017-07-28 /pmc/articles/PMC5549545/ /pubmed/28828346 http://dx.doi.org/10.4103/2277-9175.211797 Text en Copyright: © 2017 Advanced Biomedical Research 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-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Aundhakar, Swati C.
Mahajan, Sanket K.
Chhapra, Daanish A.
Hirayama's Disease: A Rare Clinical Variant of Amyotrophic Lateral Sclerosis
title Hirayama's Disease: A Rare Clinical Variant of Amyotrophic Lateral Sclerosis
title_full Hirayama's Disease: A Rare Clinical Variant of Amyotrophic Lateral Sclerosis
title_fullStr Hirayama's Disease: A Rare Clinical Variant of Amyotrophic Lateral Sclerosis
title_full_unstemmed Hirayama's Disease: A Rare Clinical Variant of Amyotrophic Lateral Sclerosis
title_short Hirayama's Disease: A Rare Clinical Variant of Amyotrophic Lateral Sclerosis
title_sort hirayama's disease: a rare clinical variant of amyotrophic lateral sclerosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5549545/
https://www.ncbi.nlm.nih.gov/pubmed/28828346
http://dx.doi.org/10.4103/2277-9175.211797
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