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The Myotonic Plot Thickens: Electrical Myotonia in Antimuscle-Specific Kinase Myasthenia Gravis

Electrical myotonia is known to occur in a number of inherited and acquired disorders including myotonic dystrophies, channelopathies, and metabolic, toxic, and inflammatory myopathies. Yet, electrical myotonia in myasthenia gravis associated with antibodies against muscle-specific tyrosine kinase (...

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Detalles Bibliográficos
Autores principales: Magnussen, Marcus, Karakis, Ioannis, Harrison, Taylor B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4681818/
https://www.ncbi.nlm.nih.gov/pubmed/26770848
http://dx.doi.org/10.1155/2015/242691
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author Magnussen, Marcus
Karakis, Ioannis
Harrison, Taylor B.
author_facet Magnussen, Marcus
Karakis, Ioannis
Harrison, Taylor B.
author_sort Magnussen, Marcus
collection PubMed
description Electrical myotonia is known to occur in a number of inherited and acquired disorders including myotonic dystrophies, channelopathies, and metabolic, toxic, and inflammatory myopathies. Yet, electrical myotonia in myasthenia gravis associated with antibodies against muscle-specific tyrosine kinase (MuSK) has not been previously reported. We describe two such patients, both of whom had a typical presentation of proximal muscle weakness with respiratory failure in the context of a significant electrodecrement in repetitive nerve stimulation. In both cases, concentric needle examination revealed electrical myotonia combined with myopathic motor unit morphology and early recruitment. These findings suggest that MuSK myasthenia should be included within the differential diagnosis of disorders with electrical myotonia.
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spelling pubmed-46818182016-01-14 The Myotonic Plot Thickens: Electrical Myotonia in Antimuscle-Specific Kinase Myasthenia Gravis Magnussen, Marcus Karakis, Ioannis Harrison, Taylor B. Case Rep Neurol Med Case Report Electrical myotonia is known to occur in a number of inherited and acquired disorders including myotonic dystrophies, channelopathies, and metabolic, toxic, and inflammatory myopathies. Yet, electrical myotonia in myasthenia gravis associated with antibodies against muscle-specific tyrosine kinase (MuSK) has not been previously reported. We describe two such patients, both of whom had a typical presentation of proximal muscle weakness with respiratory failure in the context of a significant electrodecrement in repetitive nerve stimulation. In both cases, concentric needle examination revealed electrical myotonia combined with myopathic motor unit morphology and early recruitment. These findings suggest that MuSK myasthenia should be included within the differential diagnosis of disorders with electrical myotonia. Hindawi Publishing Corporation 2015 2015-12-03 /pmc/articles/PMC4681818/ /pubmed/26770848 http://dx.doi.org/10.1155/2015/242691 Text en Copyright © 2015 Marcus Magnussen et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Magnussen, Marcus
Karakis, Ioannis
Harrison, Taylor B.
The Myotonic Plot Thickens: Electrical Myotonia in Antimuscle-Specific Kinase Myasthenia Gravis
title The Myotonic Plot Thickens: Electrical Myotonia in Antimuscle-Specific Kinase Myasthenia Gravis
title_full The Myotonic Plot Thickens: Electrical Myotonia in Antimuscle-Specific Kinase Myasthenia Gravis
title_fullStr The Myotonic Plot Thickens: Electrical Myotonia in Antimuscle-Specific Kinase Myasthenia Gravis
title_full_unstemmed The Myotonic Plot Thickens: Electrical Myotonia in Antimuscle-Specific Kinase Myasthenia Gravis
title_short The Myotonic Plot Thickens: Electrical Myotonia in Antimuscle-Specific Kinase Myasthenia Gravis
title_sort myotonic plot thickens: electrical myotonia in antimuscle-specific kinase myasthenia gravis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4681818/
https://www.ncbi.nlm.nih.gov/pubmed/26770848
http://dx.doi.org/10.1155/2015/242691
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