Association of chorea and motor neuron disease
Identifieur interne : 004568 ( Main/Exploration ); précédent : 004567; suivant : 004569Association of chorea and motor neuron disease
Auteurs : Pierre-François Pradat [France] ; François Salachas [France] ; Lucette Lacomblez [France] ; Nathalie Patte [France] ; Nadine Leforestier [France] ; Véronique Gaura [France] ; Vincent Meininger [France]Source :
- Movement Disorders [ 0885-3185 ] ; 2002-03.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Homme.
English descriptors
- KwdEn :
- Adult, Amyotrophic lateral sclerosis, Atrophy, Brain (pathology), Case study, Chorea, Chorea (diagnosis), Concomitant disease, Differential diagnostic, Follow-Up Studies, Human, Humans, Magnetic Resonance Imaging, Male, Motor Neuron Disease (diagnosis), Motor neuron disease, Neurologic Examination, Nuclear magnetic resonance imaging, Video recording.
- MESH :
- diagnosis : Chorea, Motor Neuron Disease.
- pathology : Brain.
- Adult, Atrophy, Follow-Up Studies, Humans, Magnetic Resonance Imaging, Male, Neurologic Examination.
Abstract
Amyotrophic lateral sclerosis (ALS) is classically characterized by the presence of symptoms or signs of upper and lower motor neuron impairment and sparing of other neuronal systems.1 We report on a patient who was primarily diagnosed as typical ALS and developed chorea 10 years after the onset of motor neuron signs. © 2002 Movement Disorder Society.
Url:
DOI: 10.1002/mds.10039
Affiliations:
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Le document en format XML
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<author><name sortKey="Gaura, Veronique" sort="Gaura, Veronique" uniqKey="Gaura V" first="Véronique" last="Gaura">Véronique Gaura</name>
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<term>Amyotrophic lateral sclerosis</term>
<term>Atrophy</term>
<term>Brain (pathology)</term>
<term>Case study</term>
<term>Chorea</term>
<term>Chorea (diagnosis)</term>
<term>Concomitant disease</term>
<term>Differential diagnostic</term>
<term>Follow-Up Studies</term>
<term>Human</term>
<term>Humans</term>
<term>Magnetic Resonance Imaging</term>
<term>Male</term>
<term>Motor Neuron Disease (diagnosis)</term>
<term>Motor neuron disease</term>
<term>Neurologic Examination</term>
<term>Nuclear magnetic resonance imaging</term>
<term>Video recording</term>
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<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Chorea</term>
<term>Motor Neuron Disease</term>
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<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Brain</term>
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<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
<term>Atrophy</term>
<term>Follow-Up Studies</term>
<term>Humans</term>
<term>Magnetic Resonance Imaging</term>
<term>Male</term>
<term>Neurologic Examination</term>
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<keywords scheme="Pascal" xml:lang="fr"><term>Association morbide</term>
<term>Chorée syndrome</term>
<term>Diagnostic différentiel</term>
<term>Enregistrement vidéo</term>
<term>Etude cas</term>
<term>Homme</term>
<term>Imagerie RMN</term>
<term>Neurone moteur maladie</term>
<term>Sclérose latérale amyotrophique</term>
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<front><div type="abstract" xml:lang="en">Amyotrophic lateral sclerosis (ALS) is classically characterized by the presence of symptoms or signs of upper and lower motor neuron impairment and sparing of other neuronal systems.1 We report on a patient who was primarily diagnosed as typical ALS and developed chorea 10 years after the onset of motor neuron signs. © 2002 Movement Disorder Society.</div>
</front>
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<tree><country name="France"><noRegion><name sortKey="Pradat, Pierre Rancois" sort="Pradat, Pierre Rancois" uniqKey="Pradat P" first="Pierre-François" last="Pradat">Pierre-François Pradat</name>
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<name sortKey="Gaura, Veronique" sort="Gaura, Veronique" uniqKey="Gaura V" first="Véronique" last="Gaura">Véronique Gaura</name>
<name sortKey="Lacomblez, Lucette" sort="Lacomblez, Lucette" uniqKey="Lacomblez L" first="Lucette" last="Lacomblez">Lucette Lacomblez</name>
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<name sortKey="Patte, Nathalie" sort="Patte, Nathalie" uniqKey="Patte N" first="Nathalie" last="Patte">Nathalie Patte</name>
<name sortKey="Salachas, Francois" sort="Salachas, Francois" uniqKey="Salachas F" first="François" last="Salachas">François Salachas</name>
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