Secondary dystonia – clinical clues and syndromic associations
Identifieur interne : 005C41 ( Istex/Curation ); précédent : 005C40; suivant : 005C42Secondary dystonia – clinical clues and syndromic associations
Auteurs : S. A. Schneider [Royaume-Uni, Allemagne] ; K. P. Bhatia [Royaume-Uni]Source :
- European Journal of Neurology [ 1351-5101 ] ; 2010-07.
Descripteurs français
- Wicri :
- topic : Neurologie.
English descriptors
- KwdEn :
- Ataxia, Ataxia telangiectasia, Autosomal, Basal, Basal ganglia, Bhatia, Brain iron accumulation, Clinical clues, Disord, Dystonia, Dystonic, Efns european journal, Focal dystonia, Ganglion, Gene, Globus pallidus, Iron deposition, Journal compilation, Lesion, Movement disorder, Movement disorders, Mutation, Neurodegeneration, Neurol, Neurol neurosurg psychiatry, Neurology, Neuropathy, Parkinsonism, Peripheral neuropathy, Pkan, Primary dystonia, Primary dystonias, Progressive dementia, Recessive, Retinitis pigmentosa, Schneider, Secondary dystonia, Suppl, Supranuclear, Supranuclear gaze palsy, Syndrome, Syndromic, Syndromic associations, Tardive dystonia.
- Teeft :
- Ataxia, Ataxia telangiectasia, Autosomal, Basal, Basal ganglia, Bhatia, Brain iron accumulation, Clinical clues, Disord, Dystonia, Dystonic, Efns european journal, Focal dystonia, Ganglion, Gene, Globus pallidus, Iron deposition, Journal compilation, Lesion, Movement disorder, Movement disorders, Mutation, Neurodegeneration, Neurol, Neurol neurosurg psychiatry, Neurology, Neuropathy, Parkinsonism, Peripheral neuropathy, Pkan, Primary dystonia, Primary dystonias, Progressive dementia, Recessive, Retinitis pigmentosa, Schneider, Secondary dystonia, Suppl, Supranuclear, Supranuclear gaze palsy, Syndrome, Syndromic, Syndromic associations, Tardive dystonia.
Abstract
Dystonic syndromes can be divided into primary and secondary forms. Diagnosis of secondary dystonic syndromes can be challenging as causes are multifold. They include brain lesions of various origins, metabolic disease, neurodegenerative conditions, or following exposure to drugs or toxins. However, characteristic investigational findings may be directive in the diagnostic process and facilitate making the correct diagnosis and thus allow initiating the ideal treatment. In this article, we point out some clinical clues and syndromic associations which may be helpful in the approach to a patient with dystonia.
Url:
DOI: 10.1111/j.1468-1331.2010.03051.x
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ISTEX:B9AA565BC264D5902BF2BBE9B5835B029A348FC1Le document en format XML
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<term>Basal ganglia</term>
<term>Bhatia</term>
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<term>Clinical clues</term>
<term>Disord</term>
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<term>Focal dystonia</term>
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<term>Journal compilation</term>
<term>Lesion</term>
<term>Movement disorder</term>
<term>Movement disorders</term>
<term>Mutation</term>
<term>Neurodegeneration</term>
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<term>Syndromic associations</term>
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<term>Lesion</term>
<term>Movement disorder</term>
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<term>Mutation</term>
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<term>Peripheral neuropathy</term>
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<term>Primary dystonias</term>
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<front><div type="abstract" xml:lang="en">Dystonic syndromes can be divided into primary and secondary forms. Diagnosis of secondary dystonic syndromes can be challenging as causes are multifold. They include brain lesions of various origins, metabolic disease, neurodegenerative conditions, or following exposure to drugs or toxins. However, characteristic investigational findings may be directive in the diagnostic process and facilitate making the correct diagnosis and thus allow initiating the ideal treatment. In this article, we point out some clinical clues and syndromic associations which may be helpful in the approach to a patient with dystonia.</div>
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