Dystonia in Wilson's disease
Identifieur interne : 004822 ( Main/Exploration ); précédent : 004821; suivant : 004823Dystonia in Wilson's disease
Auteurs : Marina Svetel [Yougoslavie] ; Duško Kozi [Yougoslavie] ; Elka Stefanova [Yougoslavie] ; Robert Semnic [Yougoslavie] ; Nataša Dragaševi [Yougoslavie] ; Vladimir S. Kosti [Yougoslavie]Source :
- Movement Disorders [ 0885-3185 ] ; 2001-07.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Homme.
English descriptors
- KwdEn :
- Adult, Brain (vertebrata), Concomitant disease, Dystonia, Dystonia (diagnosis), Enzymopathy, Epidemiology, Female, Frequency, Hepatolenticular Degeneration (diagnosis), Human, Humans, MRI, Magnetic Resonance Imaging, Male, Middle Aged, Neurologic Examination, Nuclear magnetic resonance imaging, Putamen, Putamen (pathology), Symptomatology, Wilson disease, Wilson's disease, dystonia, putamen.
- MESH :
- diagnosis : Dystonia, Hepatolenticular Degeneration.
- pathology : Putamen.
- Adult, Female, Humans, Magnetic Resonance Imaging, Male, Middle Aged, Neurologic Examination.
Abstract
The frequency and type of dystonic movements, as well as brain abnormalities, as depicted with magnetic resonance imaging (MRI), which might correlate with dystonia, were studied in 27 consecutive patients with a neurologic form of Wilson's disease (WD) and optimized treatment. Dystonia was found in 10 patients (37%), being generalized in half of them, while two patients had segmental, two patients multifocal dystonia, and one patient bilateral foot dystonia. Dystonia was a presenting sign in four patients and developed later in the course of the disease in six patients, despite the administered therapy for WD. Putamen was the only structure significantly more frequently lesioned in dystonic (80%) in comparison to WD patients without dystonia (24%), suggesting a relation between abnormalities in this brain region and dystonic movements in WD. © 2001 Movement Disorder Society.
Url:
DOI: 10.1002/mds.1118
Affiliations:
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Le document en format XML
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<series><title level="j">Movement Disorders</title>
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<term>Concomitant disease</term>
<term>Dystonia</term>
<term>Dystonia (diagnosis)</term>
<term>Enzymopathy</term>
<term>Epidemiology</term>
<term>Female</term>
<term>Frequency</term>
<term>Hepatolenticular Degeneration (diagnosis)</term>
<term>Human</term>
<term>Humans</term>
<term>MRI</term>
<term>Magnetic Resonance Imaging</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Neurologic Examination</term>
<term>Nuclear magnetic resonance imaging</term>
<term>Putamen</term>
<term>Putamen (pathology)</term>
<term>Symptomatology</term>
<term>Wilson disease</term>
<term>Wilson's disease</term>
<term>dystonia</term>
<term>putamen</term>
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<term>Hepatolenticular Degeneration</term>
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<term>Female</term>
<term>Humans</term>
<term>Magnetic Resonance Imaging</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Neurologic Examination</term>
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<term>Dystonie</term>
<term>Encéphale</term>
<term>Enzymopathie</term>
<term>Epidémiologie</term>
<term>Fréquence</term>
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<term>Putamen</term>
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<front><div type="abstract" xml:lang="en">The frequency and type of dystonic movements, as well as brain abnormalities, as depicted with magnetic resonance imaging (MRI), which might correlate with dystonia, were studied in 27 consecutive patients with a neurologic form of Wilson's disease (WD) and optimized treatment. Dystonia was found in 10 patients (37%), being generalized in half of them, while two patients had segmental, two patients multifocal dystonia, and one patient bilateral foot dystonia. Dystonia was a presenting sign in four patients and developed later in the course of the disease in six patients, despite the administered therapy for WD. Putamen was the only structure significantly more frequently lesioned in dystonic (80%) in comparison to WD patients without dystonia (24%), suggesting a relation between abnormalities in this brain region and dystonic movements in WD. © 2001 Movement Disorder Society.</div>
</front>
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<affiliations><list><country><li>Yougoslavie</li>
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<tree><country name="Yougoslavie"><noRegion><name sortKey="Svetel, Marina" sort="Svetel, Marina" uniqKey="Svetel M" first="Marina" last="Svetel">Marina Svetel</name>
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<name sortKey="Dragasevi, Natasa" sort="Dragasevi, Natasa" uniqKey="Dragasevi N" first="Nataša" last="Dragaševi">Nataša Dragaševi</name>
<name sortKey="Kosti, Vladimir S" sort="Kosti, Vladimir S" uniqKey="Kosti V" first="Vladimir S." last="Kosti">Vladimir S. Kosti</name>
<name sortKey="Kozi, Dusko" sort="Kozi, Dusko" uniqKey="Kozi D" first="Duško" last="Kozi">Duško Kozi</name>
<name sortKey="Semnic, Robert" sort="Semnic, Robert" uniqKey="Semnic R" first="Robert" last="Semnic">Robert Semnic</name>
<name sortKey="Stefanova, Elka" sort="Stefanova, Elka" uniqKey="Stefanova E" first="Elka" last="Stefanova">Elka Stefanova</name>
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