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Myotonic disorders: A review article

The myotonic disorders are a heterogeneous group of genetically determined diseases that are unified by the presence of myotonia, which is defined as failure of muscle relaxation after activation. The presentation of these disorders can range from asymptomatic electrical myotonia, as seen in some fo...

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Detalles Bibliográficos
Autores principales: Hahn, Chris, Salajegheh, Mohammad Kian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4852070/
https://www.ncbi.nlm.nih.gov/pubmed/27141276
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author Hahn, Chris
Salajegheh, Mohammad Kian
author_facet Hahn, Chris
Salajegheh, Mohammad Kian
author_sort Hahn, Chris
collection PubMed
description The myotonic disorders are a heterogeneous group of genetically determined diseases that are unified by the presence of myotonia, which is defined as failure of muscle relaxation after activation. The presentation of these disorders can range from asymptomatic electrical myotonia, as seen in some forms of myotonia congenita (MC), to severe disability with muscle weakness, cardiac conduction defects, and other systemic features as in myotonic dystrophy type I (DM1). In this review, we describe the clinical features and pathophysiology of the different myotonic disorders, their laboratory and electrophysiologic findings and briefly review the currently available treatments.
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spelling pubmed-48520702016-05-02 Myotonic disorders: A review article Hahn, Chris Salajegheh, Mohammad Kian Iran J Neurol Review Article The myotonic disorders are a heterogeneous group of genetically determined diseases that are unified by the presence of myotonia, which is defined as failure of muscle relaxation after activation. The presentation of these disorders can range from asymptomatic electrical myotonia, as seen in some forms of myotonia congenita (MC), to severe disability with muscle weakness, cardiac conduction defects, and other systemic features as in myotonic dystrophy type I (DM1). In this review, we describe the clinical features and pathophysiology of the different myotonic disorders, their laboratory and electrophysiologic findings and briefly review the currently available treatments. Tehran University of Medical Sciences 2016-01-05 /pmc/articles/PMC4852070/ /pubmed/27141276 Text en Copyright © 2015 Iranian Neurological Association, and Tehran University of Medical Sciences This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Hahn, Chris
Salajegheh, Mohammad Kian
Myotonic disorders: A review article
title Myotonic disorders: A review article
title_full Myotonic disorders: A review article
title_fullStr Myotonic disorders: A review article
title_full_unstemmed Myotonic disorders: A review article
title_short Myotonic disorders: A review article
title_sort myotonic disorders: a review article
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4852070/
https://www.ncbi.nlm.nih.gov/pubmed/27141276
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