A case of postanoxic encephalopathy with cortical action and brainstem reticular reflex myoclonus.
Identifieur interne : 004E59 ( PubMed/Checkpoint ); précédent : 004E58; suivant : 004E60A case of postanoxic encephalopathy with cortical action and brainstem reticular reflex myoclonus.
Auteurs : P. Brown [Royaume-Uni] ; P D Thompson ; J C Rothwell ; B L Day ; C D MarsdenSource :
- Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 1991.
English descriptors
- KwdEn :
- Aged, Arousal (physiology), Brain Mapping, Brain Stem (physiopathology), Cerebral Cortex (physiopathology), Electroencephalography, Electromyography, Epilepsies, Myoclonic (physiopathology), Female, Humans, Hypoxia, Brain (physiopathology), Motor Neurons (physiology), Myoclonus (physiopathology), Neck Muscles (innervation), Neural Pathways (physiopathology), Reaction Time (physiology), Reflex, Startle (physiology), Reticular Formation (physiopathology), Spinal Cord (physiopathology).
- MESH :
- innervation : Neck Muscles.
- physiology : Arousal, Motor Neurons, Reaction Time, Reflex, Startle.
- physiopathology : Brain Stem, Cerebral Cortex, Epilepsies, Myoclonic, Hypoxia, Brain, Myoclonus, Neural Pathways, Reticular Formation, Spinal Cord.
- Aged, Brain Mapping, Electroencephalography, Electromyography, Female, Humans.
Abstract
A patient with postanoxic encephalopathy, with both action- and stimulus-sensitive reflex myoclonus, is described. The action myoclonus was multifocal and cortical in origin. In contrast, reflex myoclonus elicited by somaesthetic and auditory stimulation was generalised. The earliest reflex electromyograph activity was recorded in the sternocleidomastoid; myoclonic activity then spread up the brainstem and down the spinal cord, suggesting that this reflex myoclonus had its origin in the caudal brainstem. Stimulus sensitivity was greatest in the limbs. The bulbospinal motor pathways involved in the generalised reflex myoclonus were rapidly conducting, and this characteristic distinguishes this form of brainstem reflex myoclonus from that described in hyperekplexia.
DOI: 10.1002/mds.870060209
PubMed: 1905387
Affiliations:
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pubmed:1905387Le document en format XML
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<author><name sortKey="Brown, P" sort="Brown, P" uniqKey="Brown P" first="P" last="Brown">P. Brown</name>
<affiliation wicri:level="2"><nlm:affiliation>MRC Human Movement and Balance Unit, Institute of Neurology, London, England.</nlm:affiliation>
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<wicri:cityArea>MRC Human Movement and Balance Unit, Institute of Neurology, London</wicri:cityArea>
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<author><name sortKey="Thompson, P D" sort="Thompson, P D" uniqKey="Thompson P" first="P D" last="Thompson">P D Thompson</name>
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<author><name sortKey="Rothwell, J C" sort="Rothwell, J C" uniqKey="Rothwell J" first="J C" last="Rothwell">J C Rothwell</name>
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<author><name sortKey="Day, B L" sort="Day, B L" uniqKey="Day B" first="B L" last="Day">B L Day</name>
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<author><name sortKey="Marsden, C D" sort="Marsden, C D" uniqKey="Marsden C" first="C D" last="Marsden">C D Marsden</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">A case of postanoxic encephalopathy with cortical action and brainstem reticular reflex myoclonus.</title>
<author><name sortKey="Brown, P" sort="Brown, P" uniqKey="Brown P" first="P" last="Brown">P. Brown</name>
<affiliation wicri:level="2"><nlm:affiliation>MRC Human Movement and Balance Unit, Institute of Neurology, London, England.</nlm:affiliation>
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<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aged</term>
<term>Arousal (physiology)</term>
<term>Brain Mapping</term>
<term>Brain Stem (physiopathology)</term>
<term>Cerebral Cortex (physiopathology)</term>
<term>Electroencephalography</term>
<term>Electromyography</term>
<term>Epilepsies, Myoclonic (physiopathology)</term>
<term>Female</term>
<term>Humans</term>
<term>Hypoxia, Brain (physiopathology)</term>
<term>Motor Neurons (physiology)</term>
<term>Myoclonus (physiopathology)</term>
<term>Neck Muscles (innervation)</term>
<term>Neural Pathways (physiopathology)</term>
<term>Reaction Time (physiology)</term>
<term>Reflex, Startle (physiology)</term>
<term>Reticular Formation (physiopathology)</term>
<term>Spinal Cord (physiopathology)</term>
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<keywords scheme="MESH" qualifier="innervation" xml:lang="en"><term>Neck Muscles</term>
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<keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Arousal</term>
<term>Motor Neurons</term>
<term>Reaction Time</term>
<term>Reflex, Startle</term>
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<keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Brain Stem</term>
<term>Cerebral Cortex</term>
<term>Epilepsies, Myoclonic</term>
<term>Hypoxia, Brain</term>
<term>Myoclonus</term>
<term>Neural Pathways</term>
<term>Reticular Formation</term>
<term>Spinal Cord</term>
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<keywords scheme="MESH" xml:lang="en"><term>Aged</term>
<term>Brain Mapping</term>
<term>Electroencephalography</term>
<term>Electromyography</term>
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<front><div type="abstract" xml:lang="en">A patient with postanoxic encephalopathy, with both action- and stimulus-sensitive reflex myoclonus, is described. The action myoclonus was multifocal and cortical in origin. In contrast, reflex myoclonus elicited by somaesthetic and auditory stimulation was generalised. The earliest reflex electromyograph activity was recorded in the sternocleidomastoid; myoclonic activity then spread up the brainstem and down the spinal cord, suggesting that this reflex myoclonus had its origin in the caudal brainstem. Stimulus sensitivity was greatest in the limbs. The bulbospinal motor pathways involved in the generalised reflex myoclonus were rapidly conducting, and this characteristic distinguishes this form of brainstem reflex myoclonus from that described in hyperekplexia.</div>
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<Issue>2</Issue>
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<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
<ISOAbbreviation>Mov. Disord.</ISOAbbreviation>
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<ArticleTitle>A case of postanoxic encephalopathy with cortical action and brainstem reticular reflex myoclonus.</ArticleTitle>
<Pagination><MedlinePgn>139-44</MedlinePgn>
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<Abstract><AbstractText>A patient with postanoxic encephalopathy, with both action- and stimulus-sensitive reflex myoclonus, is described. The action myoclonus was multifocal and cortical in origin. In contrast, reflex myoclonus elicited by somaesthetic and auditory stimulation was generalised. The earliest reflex electromyograph activity was recorded in the sternocleidomastoid; myoclonic activity then spread up the brainstem and down the spinal cord, suggesting that this reflex myoclonus had its origin in the caudal brainstem. Stimulus sensitivity was greatest in the limbs. The bulbospinal motor pathways involved in the generalised reflex myoclonus were rapidly conducting, and this characteristic distinguishes this form of brainstem reflex myoclonus from that described in hyperekplexia.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Brown</LastName>
<ForeName>P</ForeName>
<Initials>P</Initials>
<AffiliationInfo><Affiliation>MRC Human Movement and Balance Unit, Institute of Neurology, London, England.</Affiliation>
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<Author ValidYN="Y"><LastName>Thompson</LastName>
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<Author ValidYN="Y"><LastName>Rothwell</LastName>
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