Characteristic head drops and axial extension in advanced chorea‐acanthocytosis
Identifieur interne : 001E05 ( Main/Exploration ); précédent : 001E04; suivant : 001E06Characteristic head drops and axial extension in advanced chorea‐acanthocytosis
Auteurs : Susanne A. Schneider [Royaume-Uni, Allemagne] ; Anthony E. Lang [Canada] ; Elena Moro [Canada] ; Benedikt Bader [Allemagne] ; Adrian Danek [Allemagne] ; Kailash P. Bhatia [Royaume-Uni]Source :
- Movement Disorders [ 0885-3185 ] ; 2010-07-30.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
- Acanthocytosis, Adult, Chorea, Follow-Up Studies, Head, Head Movements (physiology), Humans, Middle Aged, Nervous system diseases, Neuroacanthocytosis (complications), Neuroacanthocytosis (pathology), Spasm (etiology), Trunk, acanthocytes, chorea‐acanthocytosis, head drops, neuroacanthocytosis, orobulbar features, trunk extension, trunk flexion.
- MESH :
- complications : Neuroacanthocytosis.
- etiology : Spasm.
- pathology : Neuroacanthocytosis.
- physiology : Head Movements.
- Adult, Follow-Up Studies, Humans, Middle Aged.
Abstract
Chorea‐acanthocytosis is a rare autosomal recessive neurodegenerative disorder with a complex clinical presentation comprising of a mixed movement disorder (mostly chorea and dystonia), seizures, neuropathy and myopathy, autonomic features as well as dementia and psychiatric features. Because the differential diagnosis is wide, clinical clues and red flags are important. We report here our observation of characteristic neck and trunk flexion and extension spasms in four cases with advanced chorea‐acanthocytosis. © 2010 Movement Disorder Society
Url:
DOI: 10.1002/mds.23052
Affiliations:
- Allemagne, Canada, Royaume-Uni
- Angleterre, Bavière, District de Haute-Bavière, Grand Londres, Ontario
- Londres, Munich, Toronto
- Université Louis-et-Maximilien de Munich, Université de Toronto
Links toward previous steps (curation, corpus...)
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Le document en format XML
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<front><div type="abstract" xml:lang="en">Chorea‐acanthocytosis is a rare autosomal recessive neurodegenerative disorder with a complex clinical presentation comprising of a mixed movement disorder (mostly chorea and dystonia), seizures, neuropathy and myopathy, autonomic features as well as dementia and psychiatric features. Because the differential diagnosis is wide, clinical clues and red flags are important. We report here our observation of characteristic neck and trunk flexion and extension spasms in four cases with advanced chorea‐acanthocytosis. © 2010 Movement Disorder Society</div>
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