MovDisordV3, Main, Exploration, bibRecord, 003F78

Pure cerebello‐olivary degeneration of Marie, Foix, and Alajouanine presenting with progressive cerebellar ataxia, cognitive decline, and chorea

Identifieur interne : 003F78 ( Main/Exploration ); précédent : 003F77; suivant : 003F79

Pure cerebello‐olivary degeneration of Marie, Foix, and Alajouanine presenting with progressive cerebellar ataxia, cognitive decline, and chorea

Auteurs : Susan H. Fox ; Anette Nieves [Canada, États-Unis] ; Catherine Bergeron [Canada] ; Anthony E. Lang [Canada]

Source :

Movement Disorders [ 0885-3185 ] ; 2003-12.

RBID : ISTEX:7968E3749B69AD799838EA2A2B0A566610F20BE4

Descripteurs français

Pascal (Inist)
- Ataxie cérébelleuse, Atrophie, Cervelet, Chorée syndrome, Diagnostic, Etude cas, Femelle, Hérédodégénérescence spinocérébelleuse, Olive inférieure, Personne âgée, Phénotype, Trouble cognition.
Wicri :
- topic : Personne âgée.

English descriptors

KwdEn :
- Atrophy, Brain (pathology), Case study, Cerebellar ataxia, Cerebellum, Chorea, Chorea (complications), Chorea (diagnosis), Cognition Disorders (complications), Cognition Disorders (diagnosis), Cognitive disorder, Diagnosis, Diagnosis, Differential, Elderly, Fatal Outcome, Female, Humans, Inferior olivary complex, Magnetic Resonance Imaging, Male, Middle Aged, Multiple System Atrophy (pathology), Olivopontocerebellar Atrophies (classification), Olivopontocerebellar Atrophies (complications), Olivopontocerebellar Atrophies (diagnosis), Phenotype, Severity of Illness Index, Spinocerebellar Degenerations (complications), Spinocerebellar Degenerations (diagnosis), Spinocerebellar heredodegeneration, cerebellar ataxia, chorea.
MESH :
- classification : Olivopontocerebellar Atrophies.
- complications : Chorea, Cognition Disorders, Olivopontocerebellar Atrophies, Spinocerebellar Degenerations.
- diagnosis : Chorea, Cognition Disorders, Olivopontocerebellar Atrophies, Spinocerebellar Degenerations.
- pathology : Brain, Multiple System Atrophy.
- Diagnosis, Differential, Fatal Outcome, Humans, Magnetic Resonance Imaging, Male, Middle Aged, Severity of Illness Index.

Abstract

Parenchymatous cerebellar cortical atrophy (CCA) usually presents with a “pure” cerebellar ataxia. We describe a patient with a sporadic, late‐onset progressive cerebellar ataxia plus cognitive decline and chorea who had CCA at post mortem. We discuss this unique case in the current context of classification of idiopathic cerebellar ataxia. © 2003 Movement Disorder Society

Url:

https://api.istex.fr/document/7968E3749B69AD799838EA2A2B0A566610F20BE4/fulltext/pdf

DOI: 10.1002/mds.10606

Affiliations:

Le document en format XML

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<front><div type="abstract" xml:lang="en">Parenchymatous cerebellar cortical atrophy (CCA) usually presents with a “pure” cerebellar ataxia. We describe a patient with a sporadic, late‐onset progressive cerebellar ataxia plus cognitive decline and chorea who had CCA at post mortem. We discuss this unique case in the current context of classification of idiopathic cerebellar ataxia. © 2003 Movement Disorder Society</div>
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Movement Disorders (revue)

Pure cerebello‐olivary degeneration of Marie, Foix, and Alajouanine presenting with progressive cerebellar ataxia, cognitive decline, and chorea

Pure cerebello‐olivary degeneration of Marie, Foix, and Alajouanine presenting with progressive cerebellar ataxia, cognitive decline, and chorea

Source :

Descripteurs français

English descriptors

Abstract

Links toward previous steps (curation, corpus...)

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

	Movement Disorders (revue)
	Attention, ce site est en cours de développement ! Attention, site généré par des moyens informatiques à partir de corpus bruts. Les informations ne sont donc pas validées.