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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Main Authors: Marcus Magnussen, Ioannis Karakis, Taylor B. Harrison
Format: Article
Language:English
Published: Hindawi Limited 2015-01-01
Series:Case Reports in Neurological Medicine
Online Access:http://dx.doi.org/10.1155/2015/242691
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spelling doaj-1f7281c1b26145d9900c605cd51a01142020-11-24T21:17:58ZengHindawi LimitedCase Reports in Neurological Medicine2090-66682090-66762015-01-01201510.1155/2015/242691242691The Myotonic Plot Thickens: Electrical Myotonia in Antimuscle-Specific Kinase Myasthenia GravisMarcus Magnussen0Ioannis Karakis1Taylor B. Harrison2Department of Neurology, Emory University, Atlanta, GA 30329, USADepartment of Neurology, Emory University, Atlanta, GA 30329, USADepartment of Neurology, Emory University, Atlanta, GA 30329, USAElectrical 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.http://dx.doi.org/10.1155/2015/242691
collection DOAJ
language English
format Article
sources DOAJ
author Marcus Magnussen
Ioannis Karakis
Taylor B. Harrison
spellingShingle Marcus Magnussen
Ioannis Karakis
Taylor B. Harrison
The Myotonic Plot Thickens: Electrical Myotonia in Antimuscle-Specific Kinase Myasthenia Gravis
Case Reports in Neurological Medicine
author_facet Marcus Magnussen
Ioannis Karakis
Taylor B. Harrison
author_sort Marcus Magnussen
title 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_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_sort myotonic plot thickens: electrical myotonia in antimuscle-specific kinase myasthenia gravis
publisher Hindawi Limited
series Case Reports in Neurological Medicine
issn 2090-6668
2090-6676
publishDate 2015-01-01
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.
url http://dx.doi.org/10.1155/2015/242691
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