Possible sporadic rapid‐onset dystonia–parkinsonism
Identifieur interne : 004343 ( Main/Exploration ); précédent : 004342; suivant : 004344Possible sporadic rapid‐onset dystonia–parkinsonism
Auteurs : Gurutz Linazasoro [Espagne] ; Bego A Indakoetxea [Espagne] ; Javier Ruiz [Espagne] ; Nadege Van Blercom [Espagne] ; Asier Lasa [Espagne]Source :
- Movement Disorders [ 0885-3185 ] ; 2002-05.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Adulte.
English descriptors
- KwdEn :
- Adult, Antecedent, Case study, Diagnosis, Dopamine (metabolism), Dystonia, Dystonic Disorders (diagnosis), Dystonic Disorders (etiology), Female, Homovanillic Acid (cerebrospinal fluid), Humans, Onset time, Parkinson Disease (diagnosis), Parkinson Disease (etiology), Parkinsonism, Sporadic, Time Factors, Tomography, Emission-Computed, Single-Photon.
- MESH :
- chemical , cerebrospinal fluid : Homovanillic Acid.
- chemical , metabolism : Dopamine.
- diagnosis : Dystonic Disorders, Parkinson Disease.
- etiology : Dystonic Disorders, Parkinson Disease.
- Adult, Female, Humans, Time Factors, Tomography, Emission-Computed, Single-Photon.
Abstract
Rapid‐onset dystonia–parkinsonism is a hereditary disease characterized by a combination of dystonic and parkinsonian symptoms. Bulbar musculature is predominantly affected by dystonia. The onset is usually abrupt and the progression of the disease over years is minimal or absent. Homovanillic acid levels in cerebrospinal fluid can be diminished, suggesting that the pathogenesis of the disease is related to some dysfunction in dopaminergic neurotransmission. However, no abnormality has been found in positron emission tomography studies and levodopa does not improve symptoms. The genetic abnormality is not known, but evidence for linkage to markers on chromosome 19q13 has been reported. We describe the case of a woman with a clinical picture highly suggestive of rapid onset dystonia–parkinsonism (RDP) and no family history of the disease. © 2002 Movement Disorder Society.
Url:
DOI: 10.1002/mds.10103
Affiliations:
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Le document en format XML
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<term>Dystonic Disorders (diagnosis)</term>
<term>Dystonic Disorders (etiology)</term>
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<term>Parkinsonisme</term>
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<front><div type="abstract" xml:lang="en">Rapid‐onset dystonia–parkinsonism is a hereditary disease characterized by a combination of dystonic and parkinsonian symptoms. Bulbar musculature is predominantly affected by dystonia. The onset is usually abrupt and the progression of the disease over years is minimal or absent. Homovanillic acid levels in cerebrospinal fluid can be diminished, suggesting that the pathogenesis of the disease is related to some dysfunction in dopaminergic neurotransmission. However, no abnormality has been found in positron emission tomography studies and levodopa does not improve symptoms. The genetic abnormality is not known, but evidence for linkage to markers on chromosome 19q13 has been reported. We describe the case of a woman with a clinical picture highly suggestive of rapid onset dystonia–parkinsonism (RDP) and no family history of the disease. © 2002 Movement Disorder Society.</div>
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<name sortKey="Van Blercom, Nadege" sort="Van Blercom, Nadege" uniqKey="Van Blercom N" first="Nadege" last="Van Blercom">Nadege Van Blercom</name>
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