Movement Disorders (revue)

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Toward a better definition of the restless legs syndrome. The International Restless Legs Syndrome Study Group.

Identifieur interne : 004928 ( PubMed/Corpus ); précédent : 004927; suivant : 004929

Toward a better definition of the restless legs syndrome. The International Restless Legs Syndrome Study Group.

Auteurs : A S Walters

Source :

RBID : pubmed:8552117

English descriptors

Abstract

A large International Restless Legs Syndrome (RLS) Study Group has been formed. As its first task, the group has taken upon itself the role of defining the clinical features of the RLS. As minimal criteria for diagnosis, the group proposes the following four features: (a) desire to move the extremities, often associated with paresthesias/dysesthesias; (b) motor restlessness; (c) worsening of symptoms at rest with at least temporary relief by activity, and (d) worsening of symptoms in the evening or night. Other features commonly seen in RLS include sleep disturbance, periodic limb movements in sleep and similar involuntary movements while awake, a normal neurological examination in the idiopathic form, a tendency for the symptoms to be worse in middle to older age, and, in some cases, a family history suggestive of an autosomal dominant mode of inheritance.

DOI: 10.1002/mds.870100517
PubMed: 8552117

Links to Exploration step

pubmed:8552117

Le document en format XML

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<div type="abstract" xml:lang="en">A large International Restless Legs Syndrome (RLS) Study Group has been formed. As its first task, the group has taken upon itself the role of defining the clinical features of the RLS. As minimal criteria for diagnosis, the group proposes the following four features: (a) desire to move the extremities, often associated with paresthesias/dysesthesias; (b) motor restlessness; (c) worsening of symptoms at rest with at least temporary relief by activity, and (d) worsening of symptoms in the evening or night. Other features commonly seen in RLS include sleep disturbance, periodic limb movements in sleep and similar involuntary movements while awake, a normal neurological examination in the idiopathic form, a tendency for the symptoms to be worse in middle to older age, and, in some cases, a family history suggestive of an autosomal dominant mode of inheritance.</div>
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