Myoclonus in spinal dysraphism
Identifieur interne : 000451 ( France/Analysis ); précédent : 000450; suivant : 000452Myoclonus in spinal dysraphism
Auteurs : Jane E. Warren [Australie] ; Marie Vidailhet [France] ; Christopher S. Kneebone [Australie] ; Niall P. Quinn [Royaume-Uni] ; Philip D. Thompson [Australie]Source :
- Movement Disorders [ 0885-3185 ] ; 2003-08.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Enfant.
English descriptors
- KwdEn :
- Adolescent, Case study, Child, Child, Preschool, Complication, Dorsal spine, Dysraphia, Electromyography (instrumentation), Female, Humans, Lumbar spine, Magnetic Resonance Imaging, Myelomeningocele, Myoclonus, Myoclonus (diagnosis), Myoclonus (etiology), Severity of Illness Index, Spinal Cord (pathology), Spinal Dysraphism (complications), Spinal Dysraphism (diagnosis), Spine (pathology), Young adult, paralysis, segmental myoclonus, spinal dysraphism.
- MESH :
- complications : Spinal Dysraphism.
- diagnosis : Myoclonus, Spinal Dysraphism.
- etiology : Myoclonus.
- instrumentation : Electromyography.
- pathology : Spinal Cord, Spine.
- Adolescent, Child, Preschool, Female, Humans, Magnetic Resonance Imaging, Severity of Illness Index.
Abstract
Two cases of segmental myoclonus occurring in association with spinal dysraphism are described. In one, myoclonus of paralysed legs arose below a region of spinal cord lacking any normal function, illustrating the capacity of the isolated spinal cord to generate and maintain rhythmic activity independent of supraspinal influences. © 2003 Movement Disorder Society
Url:
DOI: 10.1002/mds.10469
Affiliations:
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<term>Complication</term>
<term>Dorsal spine</term>
<term>Dysraphia</term>
<term>Electromyography (instrumentation)</term>
<term>Female</term>
<term>Humans</term>
<term>Lumbar spine</term>
<term>Magnetic Resonance Imaging</term>
<term>Myelomeningocele</term>
<term>Myoclonus</term>
<term>Myoclonus (diagnosis)</term>
<term>Myoclonus (etiology)</term>
<term>Severity of Illness Index</term>
<term>Spinal Cord (pathology)</term>
<term>Spinal Dysraphism (complications)</term>
<term>Spinal Dysraphism (diagnosis)</term>
<term>Spine (pathology)</term>
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<term>paralysis</term>
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<term>spinal dysraphism</term>
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<term>Spinal Dysraphism</term>
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<keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Myoclonus</term>
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<keywords scheme="MESH" qualifier="instrumentation" xml:lang="en"><term>Electromyography</term>
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<term>Magnetic Resonance Imaging</term>
<term>Severity of Illness Index</term>
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<term>Complication</term>
<term>Dysraphie</term>
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<term>Etude cas</term>
<term>Femelle</term>
<term>Myoclonie</term>
<term>Myéloméningocèle</term>
<term>Rachis dorsal</term>
<term>Rachis lombaire</term>
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<front><div type="abstract" xml:lang="en">Two cases of segmental myoclonus occurring in association with spinal dysraphism are described. In one, myoclonus of paralysed legs arose below a region of spinal cord lacking any normal function, illustrating the capacity of the isolated spinal cord to generate and maintain rhythmic activity independent of supraspinal influences. © 2003 Movement Disorder Society</div>
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