MovDisordV3, PascalFrancis, Curation, bibRecord, 001430

Involuntary painful muscle contractions in satoyoshi syndrome : A surface electromyographic study

Identifieur interne : 001430 ( PascalFrancis/Curation ); précédent : 001429; suivant : 001431

Involuntary painful muscle contractions in satoyoshi syndrome : A surface electromyographic study

Auteurs : Gea Drost [Pays-Bas] ; Aad Verrips [Pays-Bas] ; Baziel G. M. Van Engelen [Pays-Bas] ; Dick F. Stegeman [Pays-Bas] ; Machiel J. Zwarts [Pays-Bas]

Source :

Movement disorders [ 0885-3185 ] ; 2006.

RBID : Pascal:07-0021740

Descripteurs français

Pascal (Inist)
- Système nerveux pathologie, Douleur, Contraction musculaire, Electromyographie.

English descriptors

KwdEn :
- Electromyography, Muscle contraction, Nervous system diseases, Pain.

Abstract

We report a child with Satoyoshi syndrome manifested by involuntary painful muscle contractions and alopecia. Although an autoimmune origin of Satoyoshi syndrome seems likely, its exact etiology remains as yet unknown, as is the origin of the involuntary contractions. To gain a better understanding of the electrophysiological characteristics of the involuntary contractions, we performed a surface electromyographic (EMG) study. We investigated muscle contractions in the legs using two noninvasive techniques: high-density surface EMG (HD-sEMG) recordings on one muscle, and polymyographic surface EMG (sEMG) recordings on various muscles. During the involuntary contractions, HD-sEMG showed a fourfold increase in amplitude compared to maximal voluntary contractions. These high potentials were widely distributed across the whole muscle and showed a pronounced oscillatory behavior with a frequency around 45 Hz. Polymyographic sEMG revealed that the involuntary contractions often occur simultaneously in various muscles or showed a switch of activity from one muscle to another. These findings point to hyperactivity or a disinhibition at the alpha motor neuron level, originating probably at that level, although a central origin cannot be excluded.

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A03		`1`		`@0 Mov. disord.`
A05				`@2 21`
A06				`@2 11`
A08	`01`	`1`	`ENG`	`@1 Involuntary painful muscle contractions in satoyoshi syndrome : A surface electromyographic study`
A11	`01`	`1`		`@1 DROST (Gea)`
A11	`02`	`1`		`@1 VERRIPS (Aad)`
A11	`03`	`1`		`@1 VAN ENGELEN (Baziel G. M.)`
A11	`04`	`1`		`@1 STEGEMAN (Dick F.)`
A11	`05`	`1`		`@1 ZWARTS (Machiel J.)`
A14	`01`			`@1 Department of Clinical Neurophysiology, Institute of Neurology, Radboud University Nijmegen Medical Centre @2 Nijmegen @3 NLD @Z 1 aut. @Z 4 aut. @Z 5 aut.`
A14	`02`			`@1 Neuromuscular Centre Nijmegen, Institute of Neurology, Radboud University Nijmegen Medical Centre @2 Nijmegen @3 NLD @Z 1 aut. @Z 3 aut. @Z 4 aut. @Z 5 aut.`
A14	`03`			`@1 Canisius Wilhelmina Hospital @2 Nijmegen @3 NLD @Z 2 aut.`
A20				`@1 2015-2018`
A21				`@1 2006`
A23	`01`			`@0 ENG`
A43	`01`			`@1 INIST @2 20953 @5 354000158935070370`
A44				`@0 0000 @1 © 2007 INIST-CNRS. All rights reserved.`
A45				`@0 15 ref.`
A47	`01`	`1`		`@0 07-0021740`
A60				`@1 P @3 CC`
A61				`@0 A`
A64	`01`	`1`		`@0 Movement disorders`
A66	`01`			`@0 USA`
C01	`01`		`ENG`	@0 We report a child with Satoyoshi syndrome manifested by involuntary painful muscle contractions and alopecia. Although an autoimmune origin of Satoyoshi syndrome seems likely, its exact etiology remains as yet unknown, as is the origin of the involuntary contractions. To gain a better understanding of the electrophysiological characteristics of the involuntary contractions, we performed a surface electromyographic (EMG) study. We investigated muscle contractions in the legs using two noninvasive techniques: high-density surface EMG (HD-sEMG) recordings on one muscle, and polymyographic surface EMG (sEMG) recordings on various muscles. During the involuntary contractions, HD-sEMG showed a fourfold increase in amplitude compared to maximal voluntary contractions. These high potentials were widely distributed across the whole muscle and showed a pronounced oscillatory behavior with a frequency around 45 Hz. Polymyographic sEMG revealed that the involuntary contractions often occur simultaneously in various muscles or showed a switch of activity from one muscle to another. These findings point to hyperactivity or a disinhibition at the alpha motor neuron level, originating probably at that level, although a central origin cannot be excluded.
C02	`01`	`X`		`@0 002B17`
C02	`02`	`X`		`@0 002B17D`
C02	`03`	`X`		`@0 002B17H`
C03	`01`	`X`	`FRE`	`@0 Système nerveux pathologie @5 01`
C03	`01`	`X`	`ENG`	`@0 Nervous system diseases @5 01`
C03	`01`	`X`	`SPA`	`@0 Sistema nervioso patología @5 01`
C03	`02`	`X`	`FRE`	`@0 Douleur @5 09`
C03	`02`	`X`	`ENG`	`@0 Pain @5 09`
C03	`02`	`X`	`SPA`	`@0 Dolor @5 09`
C03	`03`	`X`	`FRE`	`@0 Contraction musculaire @5 10`
C03	`03`	`X`	`ENG`	`@0 Muscle contraction @5 10`
C03	`03`	`X`	`SPA`	`@0 Contracción muscular @5 10`
C03	`04`	`X`	`FRE`	`@0 Electromyographie @5 11`
C03	`04`	`X`	`ENG`	`@0 Electromyography @5 11`
C03	`04`	`X`	`SPA`	`@0 Electromiografía @5 11`
C07	`01`	`X`	`FRE`	`@0 Electrophysiologie @5 37`
C07	`01`	`X`	`ENG`	`@0 Electrophysiology @5 37`
C07	`01`	`X`	`SPA`	`@0 Electrofisiología @5 37`
N21				`@1 010`
N44	`01`			`@1 OTO`
N82				`@1 OTO`

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<author><name sortKey="Drost, Gea" sort="Drost, Gea" uniqKey="Drost G" first="Gea" last="Drost">Gea Drost</name>
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<front><div type="abstract" xml:lang="en">We report a child with Satoyoshi syndrome manifested by involuntary painful muscle contractions and alopecia. Although an autoimmune origin of Satoyoshi syndrome seems likely, its exact etiology remains as yet unknown, as is the origin of the involuntary contractions. To gain a better understanding of the electrophysiological characteristics of the involuntary contractions, we performed a surface electromyographic (EMG) study. We investigated muscle contractions in the legs using two noninvasive techniques: high-density surface EMG (HD-sEMG) recordings on one muscle, and polymyographic surface EMG (sEMG) recordings on various muscles. During the involuntary contractions, HD-sEMG showed a fourfold increase in amplitude compared to maximal voluntary contractions. These high potentials were widely distributed across the whole muscle and showed a pronounced oscillatory behavior with a frequency around 45 Hz. Polymyographic sEMG revealed that the involuntary contractions often occur simultaneously in various muscles or showed a switch of activity from one muscle to another. These findings point to hyperactivity or a disinhibition at the alpha motor neuron level, originating probably at that level, although a central origin cannot be excluded.</div>
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<fC01 i1="01" l="ENG"><s0>We report a child with Satoyoshi syndrome manifested by involuntary painful muscle contractions and alopecia. Although an autoimmune origin of Satoyoshi syndrome seems likely, its exact etiology remains as yet unknown, as is the origin of the involuntary contractions. To gain a better understanding of the electrophysiological characteristics of the involuntary contractions, we performed a surface electromyographic (EMG) study. We investigated muscle contractions in the legs using two noninvasive techniques: high-density surface EMG (HD-sEMG) recordings on one muscle, and polymyographic surface EMG (sEMG) recordings on various muscles. During the involuntary contractions, HD-sEMG showed a fourfold increase in amplitude compared to maximal voluntary contractions. These high potentials were widely distributed across the whole muscle and showed a pronounced oscillatory behavior with a frequency around 45 Hz. Polymyographic sEMG revealed that the involuntary contractions often occur simultaneously in various muscles or showed a switch of activity from one muscle to another. These findings point to hyperactivity or a disinhibition at the alpha motor neuron level, originating probably at that level, although a central origin cannot be excluded.</s0>
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   |type=    RBID
   |clé=     Pascal:07-0021740
   |texte=   Involuntary painful muscle contractions in satoyoshi syndrome : A surface electromyographic study
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	Movement Disorders (revue)
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Movement Disorders (revue)

Involuntary painful muscle contractions in satoyoshi syndrome : A surface electromyographic study

Involuntary painful muscle contractions in satoyoshi syndrome : A surface electromyographic study

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