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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Tehran University of Medical Sciences
2016
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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. |
format | Online Article Text |
id | pubmed-4852070 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Tehran University of Medical Sciences |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT hahnchris myotonicdisordersareviewarticle AT salajeghehmohammadkian myotonicdisordersareviewarticle |