Athetosis II: the syndrome of mild athetoid cerebral palsy.
Identifieur interne : 000941 ( Ncbi/Curation ); précédent : 000940; suivant : 000942Athetosis II: the syndrome of mild athetoid cerebral palsy.
Auteurs : John G L. Morris [Australie] ; Padraic Grattan-Smith ; Stacey K. Jankelowitz ; Victor S C. Fung ; Paul D. Clouston ; Michael W. HayesSource :
- Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 2002.
English descriptors
- KwdEn :
- MESH :
- diagnosis : Cerebral Palsy, Dystonic Disorders.
- Adolescent, Adult, Disease Progression, Female, Humans, Male, Middle Aged, Neurologic Examination, Syndrome.
Abstract
We describe 8 patients who presented with continuous, irregular movements occurring independently in individual fingers and, in some cases, toes, in the setting of mild dystonia present since early childhood and not associated with major disability. The finger movements varied from low-amplitude quivering or wriggling to larger amplitude movements in the plane of abduction-adduction as well as flexion-extension; they were asymmetrical but not unilateral. Quivering or working of the facial muscles was seen in 5 patients. Most patients reported worsening of the movements over the years, but there was no other evidence of a progressive neurological disease. We classify the movement disorder as athetosis as described by Hammond and Shaw and the syndrome as mild athetoid cerebral palsy.
DOI: 10.1002/mds.10266
PubMed: 12465069
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Jankelowitz</name></author><author><name sortKey="Fung, Victor S C" sort="Fung, Victor S C" uniqKey="Fung V" first="Victor S C" last="Fung">Victor S C. Fung</name></author><author><name sortKey="Clouston, Paul D" sort="Clouston, Paul D" uniqKey="Clouston P" first="Paul D" last="Clouston">Paul D. Clouston</name></author><author><name sortKey="Hayes, Michael W" sort="Hayes, Michael W" uniqKey="Hayes M" first="Michael W" last="Hayes">Michael W. Hayes</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2002">2002</date><idno type="RBID">pubmed:12465069</idno><idno type="pmid">12465069</idno><idno type="doi">10.1002/mds.10266</idno><idno type="wicri:Area/PubMed/Corpus">003910</idno><idno type="wicri:Area/PubMed/Curation">003910</idno><idno type="wicri:Area/PubMed/Checkpoint">003B87</idno><idno type="wicri:Area/Ncbi/Merge">000941</idno><idno type="wicri:Area/Ncbi/Curation">000941</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Athetosis II: the syndrome of mild athetoid cerebral palsy.</title><author><name sortKey="Morris, John G L" sort="Morris, John G L" uniqKey="Morris J" first="John G L" last="Morris">John G L. Morris</name><affiliation wicri:level="3"><nlm:affiliation>Department of Neurology, Westmead Hospital, Sydney, Australia. jmorris@mail.usyd.edu.au</nlm:affiliation><country xml:lang="fr">Australie</country><wicri:regionArea>Department of Neurology, Westmead Hospital, Sydney</wicri:regionArea><placeName><settlement type="city">Sydney</settlement></placeName></affiliation></author><author><name sortKey="Grattan Smith, Padraic" sort="Grattan Smith, Padraic" uniqKey="Grattan Smith P" first="Padraic" last="Grattan-Smith">Padraic Grattan-Smith</name></author><author><name sortKey="Jankelowitz, Stacey K" sort="Jankelowitz, Stacey K" uniqKey="Jankelowitz S" first="Stacey K" last="Jankelowitz">Stacey K. Jankelowitz</name></author><author><name sortKey="Fung, Victor S C" sort="Fung, Victor S C" uniqKey="Fung V" first="Victor S C" last="Fung">Victor S C. Fung</name></author><author><name sortKey="Clouston, Paul D" sort="Clouston, Paul D" uniqKey="Clouston P" first="Paul D" last="Clouston">Paul D. Clouston</name></author><author><name sortKey="Hayes, Michael W" sort="Hayes, Michael W" uniqKey="Hayes M" first="Michael W" last="Hayes">Michael W. Hayes</name></author></analytic><series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title><idno type="ISSN">0885-3185</idno><imprint><date when="2002" type="published">2002</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adolescent</term><term>Adult</term><term>Cerebral Palsy (diagnosis)</term><term>Disease Progression</term><term>Dystonic Disorders (diagnosis)</term><term>Female</term><term>Humans</term><term>Male</term><term>Middle Aged</term><term>Neurologic Examination</term><term>Syndrome</term></keywords><keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Cerebral Palsy</term><term>Dystonic Disorders</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Adolescent</term><term>Adult</term><term>Disease Progression</term><term>Female</term><term>Humans</term><term>Male</term><term>Middle Aged</term><term>Neurologic Examination</term><term>Syndrome</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">We describe 8 patients who presented with continuous, irregular movements occurring independently in individual fingers and, in some cases, toes, in the setting of mild dystonia present since early childhood and not associated with major disability. The finger movements varied from low-amplitude quivering or wriggling to larger amplitude movements in the plane of abduction-adduction as well as flexion-extension; they were asymmetrical but not unilateral. Quivering or working of the facial muscles was seen in 5 patients. Most patients reported worsening of the movements over the years, but there was no other evidence of a progressive neurological disease. We classify the movement disorder as athetosis as described by Hammond and Shaw and the syndrome as mild athetoid cerebral palsy.</div></front></TEI></record>Pour manipuler ce document sous Unix (Dilib)
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