Presumed rapid eye movement behavior disorder in Machado-Joseph disease (spinocerebellar ataxia type 3).
Identifieur interne : 003972 ( PubMed/Checkpoint ); précédent : 003971; suivant : 003973Presumed rapid eye movement behavior disorder in Machado-Joseph disease (spinocerebellar ataxia type 3).
Auteurs : Joseph H. Friedman [États-Unis]Source :
- Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 2002.
English descriptors
- KwdEn :
- Adult, Aged, Dopamine (deficiency), Dopamine Plasma Membrane Transport Proteins, Female, Follow-Up Studies, Humans, Machado-Joseph Disease (diagnosis), Machado-Joseph Disease (genetics), Machado-Joseph Disease (physiopathology), Male, Membrane Glycoproteins, Membrane Transport Proteins (physiology), Middle Aged, Nerve Tissue Proteins, Neurologic Examination, Polysomnography, REM Sleep Behavior Disorder (diagnosis), REM Sleep Behavior Disorder (genetics), REM Sleep Behavior Disorder (physiopathology), Tomography, Emission-Computed, Single-Photon.
- MESH :
- chemical , deficiency : Dopamine.
- diagnosis : Machado-Joseph Disease, REM Sleep Behavior Disorder.
- genetics : Machado-Joseph Disease, REM Sleep Behavior Disorder.
- chemical , physiology : Membrane Transport Proteins.
- physiopathology : Machado-Joseph Disease, REM Sleep Behavior Disorder.
- Adult, Aged, Dopamine Plasma Membrane Transport Proteins, Female, Follow-Up Studies, Humans, Male, Membrane Glycoproteins, Middle Aged, Nerve Tissue Proteins, Neurologic Examination, Polysomnography, Tomography, Emission-Computed, Single-Photon.
Abstract
Rapid eye movement behavior disorder (RBD) is a recently recognized sleep disorder in which patients are occasionally not paralyzed during the dream portions of sleep. When not idiopathic, this state has been associated primarily with parkinsonian conditions but also with a small number of medications and other neurodegenerative disorders. Dopamine deficiency may play a role in some patients. This report describes the occurrence of a syndrome that appears to be RBD in 6 of 7 patients followed with Spinocerebellar ataxia type 3 (Machado-Joseph disease). Polysomnography was normal in 1 patient. Two of these patients had had single photon emission computed tomographic imaging of the dopamine transporter 1 year previously.
DOI: 10.1002/mds.10269
PubMed: 12465081
Affiliations:
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pubmed:12465081Le document en format XML
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<affiliation wicri:level="1"><nlm:affiliation>Department of Clinical Neurosciences, Brown University Medical School, Providence, Rhode Island 02860, USA. joseph_friedman@mhri.org</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Clinical Neurosciences, Brown University Medical School, Providence, Rhode Island 02860</wicri:regionArea>
<wicri:noRegion>Rhode Island 02860</wicri:noRegion>
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<term>Dopamine Plasma Membrane Transport Proteins</term>
<term>Female</term>
<term>Follow-Up Studies</term>
<term>Humans</term>
<term>Machado-Joseph Disease (diagnosis)</term>
<term>Machado-Joseph Disease (genetics)</term>
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<front><div type="abstract" xml:lang="en">Rapid eye movement behavior disorder (RBD) is a recently recognized sleep disorder in which patients are occasionally not paralyzed during the dream portions of sleep. When not idiopathic, this state has been associated primarily with parkinsonian conditions but also with a small number of medications and other neurodegenerative disorders. Dopamine deficiency may play a role in some patients. This report describes the occurrence of a syndrome that appears to be RBD in 6 of 7 patients followed with Spinocerebellar ataxia type 3 (Machado-Joseph disease). Polysomnography was normal in 1 patient. Two of these patients had had single photon emission computed tomographic imaging of the dopamine transporter 1 year previously.</div>
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<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
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<Abstract><AbstractText>Rapid eye movement behavior disorder (RBD) is a recently recognized sleep disorder in which patients are occasionally not paralyzed during the dream portions of sleep. When not idiopathic, this state has been associated primarily with parkinsonian conditions but also with a small number of medications and other neurodegenerative disorders. Dopamine deficiency may play a role in some patients. This report describes the occurrence of a syndrome that appears to be RBD in 6 of 7 patients followed with Spinocerebellar ataxia type 3 (Machado-Joseph disease). Polysomnography was normal in 1 patient. Two of these patients had had single photon emission computed tomographic imaging of the dopamine transporter 1 year previously.</AbstractText>
<CopyrightInformation>Copyright 2002 Movement Disorder Society</CopyrightInformation>
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<Initials>JH</Initials>
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