Dysarthria and orofacial apraxia in corticobasal degeneration
Identifieur interne : 000527 ( France/Analysis ); précédent : 000526; suivant : 000528Dysarthria and orofacial apraxia in corticobasal degeneration
Auteurs : Canan Özsancak [France] ; Pascal Auzou [France] ; Didier Hannequin [France]Source :
- Movement Disorders [ 0885-3185 ] ; 2000-09.
Descripteurs français
- Pascal (Inist)
- Wicri :
English descriptors
- KwdEn :
- Aged, Apraxia, Apraxias (etiology), Basal Ganglia Diseases (complications), Basal Ganglia Diseases (physiopathology), Basal ganglion, Cerebral Cortex (physiopathology), Cerebral cortex, Complication, Corticobasal degeneration, Degeneration, Dysarthria, Dysarthria (etiology), Face, Female, France, Frequency, Human, Humans, Male, Neurodegenerative Diseases (complications), Neurodegenerative Diseases (physiopathology), Neuropsychological Tests, Oral cavity, Orofacial apraxia, 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.
Url:
DOI: 10.1002/1531-8257(200009)15:5<905::AID-MDS1022>3.0.CO;2-D
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: 002034
- to stream Istex, to step Curation: 002034
- to stream Istex, to step Checkpoint: 003286
- to stream Main, to step Merge: 007383
- to stream PascalFrancis, to step Corpus: 002B39
- to stream PascalFrancis, to step Curation: 000182
- to stream PascalFrancis, to step Checkpoint: 002C15
- to stream Main, to step Merge: 007607
- to stream PubMed, to step Corpus: 003F07
- to stream PubMed, to step Curation: 003F07
- to stream PubMed, to step Checkpoint: 003F94
- to stream Ncbi, to step Merge: 000344
- to stream Ncbi, to step Curation: 000344
- to stream Ncbi, to step Checkpoint: 000344
- to stream Main, to step Merge: 007137
- to stream Main, to step Curation: 004A85
- to stream Main, to step Exploration: 004A85
- to stream France, to step Extraction: 000527
Links to Exploration step
ISTEX:B2A1EEC7FDDC8743C6FDF7B988ADD034BE7C98D6Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">Dysarthria and orofacial apraxia in corticobasal degeneration</title><author><name sortKey="Ozsancak, Canan" sort="Ozsancak, Canan" uniqKey="Ozsancak C" first="Canan" last="Özsancak">Canan Özsancak</name></author><author><name sortKey="Auzou, Pascal" sort="Auzou, Pascal" uniqKey="Auzou P" first="Pascal" last="Auzou">Pascal Auzou</name></author><author><name sortKey="Hannequin, Didier" sort="Hannequin, Didier" uniqKey="Hannequin D" first="Didier" last="Hannequin">Didier Hannequin</name></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:B2A1EEC7FDDC8743C6FDF7B988ADD034BE7C98D6</idno><date when="2000" year="2000">2000</date><idno type="doi">10.1002/1531-8257(200009)15:5<905::AID-MDS1022>3.0.CO;2-D</idno><idno type="url">https://api.istex.fr/document/B2A1EEC7FDDC8743C6FDF7B988ADD034BE7C98D6/fulltext/pdf</idno><idno type="wicri:Area/Istex/Corpus">002034</idno><idno type="wicri:Area/Istex/Curation">002034</idno><idno type="wicri:Area/Istex/Checkpoint">003286</idno><idno type="wicri:doubleKey">0885-3185:2000:Ozsancak C:dysarthria:and:orofacial</idno><idno type="wicri:Area/Main/Merge">007383</idno><idno type="wicri:source">INIST</idno><idno type="RBID">Pascal:00-0480777</idno><idno type="wicri:Area/PascalFrancis/Corpus">002B39</idno><idno type="wicri:Area/PascalFrancis/Curation">000182</idno><idno type="wicri:Area/PascalFrancis/Checkpoint">002C15</idno><idno type="wicri:doubleKey">0885-3185:2000:Ozsancak C:dysarthria:and:orofacial</idno><idno type="wicri:Area/Main/Merge">007607</idno><idno type="wicri:source">PubMed</idno><idno type="RBID">pubmed:11009198</idno><idno type="wicri:Area/PubMed/Corpus">003F07</idno><idno type="wicri:Area/PubMed/Curation">003F07</idno><idno type="wicri:Area/PubMed/Checkpoint">003F94</idno><idno type="wicri:Area/Ncbi/Merge">000344</idno><idno type="wicri:Area/Ncbi/Curation">000344</idno><idno type="wicri:Area/Ncbi/Checkpoint">000344</idno><idno type="wicri:doubleKey">0885-3185:2000:Ozsancak C:dysarthria:and:orofacial</idno><idno type="wicri:Area/Main/Merge">007137</idno><idno type="wicri:Area/Main/Curation">004A85</idno><idno type="wicri:Area/Main/Exploration">004A85</idno><idno type="wicri:Area/France/Extraction">000527</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Dysarthria and orofacial apraxia in corticobasal degeneration</title><author><name sortKey="Ozsancak, Canan" sort="Ozsancak, Canan" uniqKey="Ozsancak C" first="Canan" last="Özsancak">Canan Özsancak</name><affiliation wicri:level="1"><country xml:lang="fr">France</country><wicri:regionArea>Fédération des Sciences Neurologiques, Rouen</wicri:regionArea><placeName><settlement type="city">Rouen</settlement></placeName></affiliation></author><author><name sortKey="Auzou, Pascal" sort="Auzou, Pascal" uniqKey="Auzou P" first="Pascal" last="Auzou">Pascal Auzou</name><affiliation wicri:level="1"><country xml:lang="fr">France</country><wicri:regionArea>Fédération des Sciences Neurologiques, Rouen</wicri:regionArea><placeName><settlement type="city">Rouen</settlement></placeName></affiliation></author><author><name sortKey="Hannequin, Didier" sort="Hannequin, Didier" uniqKey="Hannequin D" first="Didier" last="Hannequin">Didier Hannequin</name><affiliation wicri:level="1"><country xml:lang="fr">France</country><wicri:regionArea>Fédération des Sciences Neurologiques, Rouen</wicri:regionArea><placeName><settlement type="city">Rouen</settlement></placeName></affiliation></author></analytic><monogr></monogr><series><title level="j">Movement Disorders</title><title level="j" type="abbrev">Mov. Disord.</title><idno type="ISSN">0885-3185</idno><idno type="eISSN">1531-8257</idno><imprint><publisher>John Wiley & Sons, Inc.</publisher><pubPlace>New York</pubPlace><date type="published" when="2000-09">2000-09</date><biblScope unit="vol">15</biblScope><biblScope unit="issue">5</biblScope><biblScope unit="page" from="905">905</biblScope><biblScope unit="page" to="910">910</biblScope></imprint><idno type="ISSN">0885-3185</idno></series><idno type="istex">B2A1EEC7FDDC8743C6FDF7B988ADD034BE7C98D6</idno><idno type="DOI">10.1002/1531-8257(200009)15:5<905::AID-MDS1022>3.0.CO;2-D</idno><idno type="ArticleID">MDS1022</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0885-3185</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aged</term><term>Apraxia</term><term>Apraxias (etiology)</term><term>Basal Ganglia Diseases (complications)</term><term>Basal Ganglia Diseases (physiopathology)</term><term>Basal ganglion</term><term>Cerebral Cortex (physiopathology)</term><term>Cerebral cortex</term><term>Complication</term><term>Corticobasal degeneration</term><term>Degeneration</term><term>Dysarthria</term><term>Dysarthria (etiology)</term><term>Face</term><term>Female</term><term>France</term><term>Frequency</term><term>Human</term><term>Humans</term><term>Male</term><term>Neurodegenerative Diseases (complications)</term><term>Neurodegenerative Diseases (physiopathology)</term><term>Neuropsychological Tests</term><term>Oral cavity</term><term>Orofacial apraxia</term><term>Parkinsonian Disorders (etiology)</term><term>Psychiatric Status Rating Scales</term><term>Severity of Illness Index</term><term>Speech Intelligibility</term></keywords><keywords scheme="MESH" type="geographic" xml:lang="en"><term>France</term></keywords><keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Basal Ganglia Diseases</term><term>Neurodegenerative Diseases</term></keywords><keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Apraxias</term><term>Dysarthria</term><term>Parkinsonian Disorders</term></keywords><keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Basal Ganglia Diseases</term><term>Cerebral Cortex</term><term>Neurodegenerative Diseases</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Aged</term><term>Female</term><term>Humans</term><term>Male</term><term>Neuropsychological Tests</term><term>Psychiatric Status Rating Scales</term><term>Severity of Illness Index</term><term>Speech Intelligibility</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Apraxie</term><term>Cavité buccale</term><term>Complication</term><term>Cortex cérébral</term><term>Dysarthrie</term><term>Dégénérescence</term><term>Face</term><term>Fréquence</term><term>Homme</term><term>Noyau gris central</term></keywords><keywords scheme="Wicri" type="geographic" xml:lang="fr"><term>France</term></keywords><keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Homme</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><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></TEI><affiliations><list><country><li>France</li></country><settlement><li>Rouen</li></settlement></list><tree><country name="France"><noRegion><name sortKey="Ozsancak, Canan" sort="Ozsancak, Canan" uniqKey="Ozsancak C" first="Canan" last="Özsancak">Canan Özsancak</name></noRegion><name sortKey="Auzou, Pascal" sort="Auzou, Pascal" uniqKey="Auzou P" first="Pascal" last="Auzou">Pascal Auzou</name><name sortKey="Hannequin, Didier" sort="Hannequin, Didier" uniqKey="Hannequin D" first="Didier" last="Hannequin">Didier Hannequin</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/France/Analysis
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000527 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/France/Analysis/biblio.hfd -nk 000527 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= Wicri/Santé
|area= MovDisordV3
|flux= France
|étape= Analysis
|type= RBID
|clé= ISTEX:B2A1EEC7FDDC8743C6FDF7B988ADD034BE7C98D6
|texte= Dysarthria and orofacial apraxia in corticobasal degeneration
}}
| This area was generated with Dilib version V0.6.23. |  |