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Ocular myasthenia gravis: Predictive value of single-fiber electromyography

Extraocular muscle weakness is the most common presenting sign of myasthenia gravis (MG). More than half of patients presenting with symptoms isolated to these muscles (OMG) develop generalized myasthenia gravis (GMG) over the course of their illness. No clinical, laboratory, or electrophysiological...

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Published in:Muscle & nerve 1999-09, Vol.22 (9), p.1222-1227
Main Authors: Weinberg, David H., Rizzo III, Joseph F., Hayes, Michael T., Kneeland, Michael D., Kelly Jr, John J.
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container_issue 9
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creator Weinberg, David H.
Rizzo III, Joseph F.
Hayes, Michael T.
Kneeland, Michael D.
Kelly Jr, John J.
description Extraocular muscle weakness is the most common presenting sign of myasthenia gravis (MG). More than half of patients presenting with symptoms isolated to these muscles (OMG) develop generalized myasthenia gravis (GMG) over the course of their illness. No clinical, laboratory, or electrophysiological features are recognized that identify these high‐risk patients. We have therefore assessed the ability of single‐fiber electromyography (SFEMG) to predict the development of GMG in patients presenting with OMG. Thirty‐nine consecutive patients presenting with OMG underwent SFEMG of the extensor digitorum communis muscle as well as a battery of other laboratory and imaging studies at the time of diagnosis. All patients were followed prospectively for a minimum of 24 months or until they developed GMG. Two patients were excluded, leaving 37 for assessment. Twenty remained with pure OMG for the entire follow‐up period (mean, 55 months). Twenty‐six of the 37 had abnormal SFEMG studies at presentation. Eleven of these remained with OMG and 15 developed GMG. Fifty‐eight percent of patients with an abnormal SFEMG developed GMG, whereas 82% of those with a normal study remained with OMG. Thus, a normal SFEMG was associated with MG remaining restricted to the extraocular muscles. (P = 0.036, Fisher's exact test), but an abnormal SFEMG was not predictive of subsequent development of GMG. © 1999 John Wiley & Sons, Inc. Muscle Nerve 22: 1222–1227, 1999
doi_str_mv 10.1002/(SICI)1097-4598(199909)22:9<1222::AID-MUS8>3.0.CO;2-R
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More than half of patients presenting with symptoms isolated to these muscles (OMG) develop generalized myasthenia gravis (GMG) over the course of their illness. No clinical, laboratory, or electrophysiological features are recognized that identify these high‐risk patients. We have therefore assessed the ability of single‐fiber electromyography (SFEMG) to predict the development of GMG in patients presenting with OMG. Thirty‐nine consecutive patients presenting with OMG underwent SFEMG of the extensor digitorum communis muscle as well as a battery of other laboratory and imaging studies at the time of diagnosis. All patients were followed prospectively for a minimum of 24 months or until they developed GMG. Two patients were excluded, leaving 37 for assessment. Twenty remained with pure OMG for the entire follow‐up period (mean, 55 months). Twenty‐six of the 37 had abnormal SFEMG studies at presentation. Eleven of these remained with OMG and 15 developed GMG. 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Neuromuscular diseases</topic><topic>Electromyography</topic><topic>Female</topic><topic>Fingers</topic><topic>generalized</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Muscle Fibers, Skeletal - physiology</topic><topic>myasthenia gravis</topic><topic>Myasthenia Gravis - physiopathology</topic><topic>Neurology</topic><topic>ocular</topic><topic>Ocular Motility Disorders - physiopathology</topic><topic>Oculomotor Muscles - physiopathology</topic><topic>Predictive Value of Tests</topic><topic>prognosis</topic><topic>Prospective Studies</topic><topic>single-fiber electromyography</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Weinberg, David H.</creatorcontrib><creatorcontrib>Rizzo III, Joseph F.</creatorcontrib><creatorcontrib>Hayes, Michael T.</creatorcontrib><creatorcontrib>Kneeland, Michael D.</creatorcontrib><creatorcontrib>Kelly Jr, John J.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Muscle &amp; nerve</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Weinberg, David H.</au><au>Rizzo III, Joseph F.</au><au>Hayes, Michael T.</au><au>Kneeland, Michael D.</au><au>Kelly Jr, John J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ocular myasthenia gravis: Predictive value of single-fiber electromyography</atitle><jtitle>Muscle &amp; nerve</jtitle><addtitle>Muscle Nerve</addtitle><date>1999-09</date><risdate>1999</risdate><volume>22</volume><issue>9</issue><spage>1222</spage><epage>1227</epage><pages>1222-1227</pages><issn>0148-639X</issn><eissn>1097-4598</eissn><coden>MUNEDE</coden><abstract>Extraocular muscle weakness is the most common presenting sign of myasthenia gravis (MG). 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subjects Adult
Aged
Biological and medical sciences
Disease Progression
Diseases of striated muscles. Neuromuscular diseases
Electromyography
Female
Fingers
generalized
Humans
Male
Medical sciences
Middle Aged
Muscle Fibers, Skeletal - physiology
myasthenia gravis
Myasthenia Gravis - physiopathology
Neurology
ocular
Ocular Motility Disorders - physiopathology
Oculomotor Muscles - physiopathology
Predictive Value of Tests
prognosis
Prospective Studies
single-fiber electromyography
title Ocular myasthenia gravis: Predictive value of single-fiber electromyography
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