Spinocerebellar ataxia type 2 with levodopa‐responsive parkinsonism culminating in motor neuron disease
Identifieur interne : 000382 ( Main/Curation ); précédent : 000381; suivant : 000383Spinocerebellar ataxia type 2 with levodopa‐responsive parkinsonism culminating in motor neuron disease
Auteurs : Jon Infante [Espagne] ; José Berciano [Espagne] ; Victor Volpini [Espagne] ; Jordi Corral [Espagne] ; José Miguel Polo [Espagne] ; Julio Pascual [Espagne] ; Onofre Combarros [Espagne]Source :
- Movement Disorders [ 0885-3185 ] ; 2004-07.
English descriptors
- KwdEn :
- ALS, SCA2, parkinsonism.
Abstract
We describe an exceptional spinocerebellar ataxia type 2 (SCA2) phenotype combining cerebellar ataxia, levodopa‐responsive parkinsonism, and motor neuron symptoms. We conclude that motor neuron symptoms and signs may be a striking manifestation in SCA2, masking pre‐existing cerebellar and extrapyramidal semeiology. © 2004 Movement Disorder Society
Url:
DOI: 10.1002/mds.20090
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<front><div type="abstract" xml:lang="en">We describe an exceptional spinocerebellar ataxia type 2 (SCA2) phenotype combining cerebellar ataxia, levodopa‐responsive parkinsonism, and motor neuron symptoms. We conclude that motor neuron symptoms and signs may be a striking manifestation in SCA2, masking pre‐existing cerebellar and extrapyramidal semeiology. © 2004 Movement Disorder Society</div>
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