Clinical variants of idiopathic torsion dystonia.
Identifieur interne : 000064 ( Pmc/Curation ); précédent : 000063; suivant : 000065Clinical variants of idiopathic torsion dystonia.
Auteurs : S. FahnSource :
- Journal of Neurology, Neurosurgery, and Psychiatry [ 0022-3050 ] ; 1989.
Abstract
Some patients with dystonic movements and postures not known to be caused by environmental or degenerative disorders can be segregated from classical-appearing idiopathic torsion dystonia on the basis of distinctive clinical and pharmacologic features. Many of them should be considered within the family of dystonia, as clinical variants of idiopathic torsion dystonia, while others are better classified as being part of other families of dyskinesias. In the former group are paradoxical dystonia, myoclonic dystonia, diurnal dystonia, and dopa-responsive dystonia. The latter group consists of dystonic tics and the various entities comprising paroxysmal dystonia, namely kinesigenic, nonkinesigenic and hypnogenic dystonia.
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PubMed: 2666583
PubMed Central: 1033313
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<front><journal-meta><journal-id journal-id-type="nlm-ta">J Neurol Neurosurg Psychiatry</journal-id><journal-title>Journal of Neurology, Neurosurgery, and Psychiatry</journal-title><issn pub-type="ppub">0022-3050</issn><issn pub-type="epub">1468-330X</issn></journal-meta><article-meta><article-id pub-id-type="pmid">2666583</article-id><article-id pub-id-type="pmc">1033313</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title>Clinical variants of idiopathic torsion dystonia.</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Fahn</surname><given-names>S</given-names></name></contrib></contrib-group><aff>Department of Neurology, Columbia University College of Physicians & Surgeons, New York.</aff><pub-date pub-type="ppub"><month>6</month><year>1989</year></pub-date><volume>52</volume><issue>Suppl</issue><fpage>96</fpage><lpage>100</lpage><abstract><p>Some patients with dystonic movements and postures not known to be caused by environmental or degenerative disorders can be segregated from classical-appearing idiopathic torsion dystonia on the basis of distinctive clinical and pharmacologic features. Many of them should be considered within the family of dystonia, as clinical variants of idiopathic torsion dystonia, while others are better classified as being part of other families of dyskinesias. In the former group are paradoxical dystonia, myoclonic dystonia, diurnal dystonia, and dopa-responsive dystonia. The latter group consists of dystonic tics and the various entities comprising paroxysmal dystonia, namely kinesigenic, nonkinesigenic and hypnogenic dystonia.</p></abstract></article-meta></front></pmc></record>Pour manipuler ce document sous Unix (Dilib)
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