Dysarthria and orofacial apraxia in corticobasal degeneration.
Identifieur interne : 003F07 ( PubMed/Curation ); précédent : 003F06; suivant : 003F08Dysarthria and orofacial apraxia in corticobasal degeneration.
Auteurs : C. Ozsancak [France] ; P. Auzou ; D. HannequinSource :
- Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 2000.
Descripteurs français
- Wicri :
- geographic : France.
English descriptors
- KwdEn :
- Aged, Apraxias (etiology), Basal Ganglia Diseases (complications), Basal Ganglia Diseases (physiopathology), Cerebral Cortex (physiopathology), Dysarthria (etiology), Female, France, Humans, Male, Neurodegenerative Diseases (complications), Neurodegenerative Diseases (physiopathology), Neuropsychological Tests, Parkinsonian Disorders (etiology), Psychiatric Status Rating Scales, Severity of Illness Index, Speech Intelligibility.
- MESH :
- geographic : France.
- complications : Basal Ganglia Diseases, Neurodegenerative Diseases.
- etiology : Apraxias, Dysarthria, Parkinsonian Disorders.
- physiopathology : Basal Ganglia Diseases, Cerebral Cortex, Neurodegenerative Diseases.
- Aged, Female, Humans, Male, Neuropsychological Tests, Psychiatric Status Rating Scales, Severity of Illness Index, Speech Intelligibility.
Abstract
The authors evaluated dysarthria and orofacial apraxia (OFA) in 10 patients with a clinical diagnosis of corticobasal degeneration (CBD). Nine patients were slightly dysarthric according to the French version of the Frenchay Dysarthria Assessment, which evaluates the motricity of the components of the vocal tract. The severity of dysarthria assessed by an intelligibility score was correlated to the global severity of the disease, but not to the duration of the disease. Voluntary movements of the tongue and the lips were impaired in all patients. OFA, evaluated with simple and sequential gestures, was present in nine patients. Sequential gestures were more frequently impaired. The score of OFA was not correlated to the severity of dysarthria, suggesting independent underlying mechanisms. Thus, when specifically assessed, dysarthria and OFA are more frequent in CBD than usually reported. We propose that the underlying pathophysiology is the result of a deficit in programming and execution of repetitive movements.
PubMed: 11009198
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pubmed:11009198Le document en format XML
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<author><name sortKey="Ozsancak, C" sort="Ozsancak, C" uniqKey="Ozsancak C" first="C" last="Ozsancak">C. Ozsancak</name>
<affiliation wicri:level="1"><nlm:affiliation>Fédération des Sciences Neurologiques, Rouen, France. c-ozsancak@yahoo.fr</nlm:affiliation>
<country xml:lang="fr">France</country>
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<author><name sortKey="Auzou, P" sort="Auzou, P" uniqKey="Auzou P" first="P" last="Auzou">P. Auzou</name>
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<author><name sortKey="Hannequin, D" sort="Hannequin, D" uniqKey="Hannequin D" first="D" last="Hannequin">D. Hannequin</name>
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<front><div type="abstract" xml:lang="en">The authors evaluated dysarthria and orofacial apraxia (OFA) in 10 patients with a clinical diagnosis of corticobasal degeneration (CBD). Nine patients were slightly dysarthric according to the French version of the Frenchay Dysarthria Assessment, which evaluates the motricity of the components of the vocal tract. The severity of dysarthria assessed by an intelligibility score was correlated to the global severity of the disease, but not to the duration of the disease. Voluntary movements of the tongue and the lips were impaired in all patients. OFA, evaluated with simple and sequential gestures, was present in nine patients. Sequential gestures were more frequently impaired. The score of OFA was not correlated to the severity of dysarthria, suggesting independent underlying mechanisms. Thus, when specifically assessed, dysarthria and OFA are more frequent in CBD than usually reported. We propose that the underlying pathophysiology is the result of a deficit in programming and execution of repetitive movements.</div>
</front>
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<Abstract><AbstractText>The authors evaluated dysarthria and orofacial apraxia (OFA) in 10 patients with a clinical diagnosis of corticobasal degeneration (CBD). Nine patients were slightly dysarthric according to the French version of the Frenchay Dysarthria Assessment, which evaluates the motricity of the components of the vocal tract. The severity of dysarthria assessed by an intelligibility score was correlated to the global severity of the disease, but not to the duration of the disease. Voluntary movements of the tongue and the lips were impaired in all patients. OFA, evaluated with simple and sequential gestures, was present in nine patients. Sequential gestures were more frequently impaired. The score of OFA was not correlated to the severity of dysarthria, suggesting independent underlying mechanisms. Thus, when specifically assessed, dysarthria and OFA are more frequent in CBD than usually reported. We propose that the underlying pathophysiology is the result of a deficit in programming and execution of repetitive movements.</AbstractText>
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