Subthalamic‐thalamic DBS in a case with spinocerebellar ataxia type 2 and severe tremor—A unusual clinical benefit
Identifieur interne : 003A74 ( Main/Merge ); précédent : 003A73; suivant : 003A75Subthalamic‐thalamic DBS in a case with spinocerebellar ataxia type 2 and severe tremor—A unusual clinical benefit
Auteurs : Hans-Joachim Freund [Allemagne] ; Utako B. Barnikol [Allemagne] ; Dagmar Nolte [Allemagne] ; Harald Treuer [Allemagne] ; Georg Auburger [Allemagne] ; Peter A. Tass [Allemagne] ; Madjid Samii [Allemagne] ; Volker Sturm [Allemagne]Source :
- Movement Disorders [ 0885-3185 ] ; 2007-04-15.
English descriptors
- KwdEn :
- Activities of Daily Living (classification), Adult, Deep Brain Stimulation, Electrodes, Implanted, Female, Follow-Up Studies, Humans, Neurologic Examination, Spinocerebellar Ataxias (diagnosis), Spinocerebellar Ataxias (physiopathology), Spinocerebellar Ataxias (therapy), Subthalamic Nucleus (physiopathology), Torticollis (diagnosis), Torticollis (physiopathology), Torticollis (therapy), Treatment Outcome, Tremor (diagnosis), Tremor (physiopathology), Tremor (therapy), Ventral Thalamic Nuclei (physiopathology), cerebellar tremor, deep brain stimulation, long‐lasting benefit, subthalamic target.
- MESH :
- classification : Activities of Daily Living.
- diagnosis : Spinocerebellar Ataxias, Torticollis, Tremor.
- physiopathology : Spinocerebellar Ataxias, Subthalamic Nucleus, Torticollis, Tremor, Ventral Thalamic Nuclei.
- therapy : Spinocerebellar Ataxias, Torticollis, Tremor.
- Adult, Deep Brain Stimulation, Electrodes, Implanted, Female, Follow-Up Studies, Humans, Neurologic Examination, Treatment Outcome.
Abstract
This is a single case report of a patient with spinocerebellar ataxia type 2 (SCA2) and severe tremor. Whereas disease progression with prevailing ataxia and dysmetria was slow over the first symptomatic 6 years, 6 months prior to operation were characterized by the development of a severe, debilitating postural tremor rendering the patient unable to independently sit, stand, speak, or swallow. Deep brain stimulation (DBS) at a subthalamic–thalamic electrode position almost completely arrested her tremor. The patient regained the functional state prior to her rapid disease progression allowing a restricted range of daily activities. Her condition has remained approximately stable over the two postoperative years to date. In addition to the efficacy of DBS on cerebellar tremor, the results illustrate a remarkable improvement of the patient's general condition and independence.
Url:
DOI: 10.1002/mds.21338
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<front><div type="abstract" xml:lang="en">This is a single case report of a patient with spinocerebellar ataxia type 2 (SCA2) and severe tremor. Whereas disease progression with prevailing ataxia and dysmetria was slow over the first symptomatic 6 years, 6 months prior to operation were characterized by the development of a severe, debilitating postural tremor rendering the patient unable to independently sit, stand, speak, or swallow. Deep brain stimulation (DBS) at a subthalamic–thalamic electrode position almost completely arrested her tremor. The patient regained the functional state prior to her rapid disease progression allowing a restricted range of daily activities. Her condition has remained approximately stable over the two postoperative years to date. In addition to the efficacy of DBS on cerebellar tremor, the results illustrate a remarkable improvement of the patient's general condition and independence.</div>
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<front><div type="abstract" xml:lang="en">This is a single case report of a patient with spinocerebellar ataxia type 2 (SCA2) and severe tremor. Whereas disease progression with prevailing ataxia and dysmetria was slow over the first symptomatic 6 years, 6 months prior to operation were characterized by the development of a severe, debilitating postural tremor rendering the patient unable to independently sit, stand, speak, or swallow. Deep brain stimulation (DBS) at a subthalamic–thalamic electrode position almost completely arrested her tremor. The patient regained the functional state prior to her rapid disease progression allowing a restricted range of daily activities. Her condition has remained approximately stable over the two postoperative years to date. In addition to the efficacy of DBS on cerebellar tremor, the results illustrate a remarkable improvement of the patient's general condition and independence.</div>
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<author><name sortKey="Auburger, Georg" sort="Auburger, Georg" uniqKey="Auburger G" first="Georg" last="Auburger">Georg Auburger</name>
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<author><name sortKey="Tass, Peter A" sort="Tass, Peter A" uniqKey="Tass P" first="Peter A" last="Tass">Peter A. Tass</name>
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<author><name sortKey="Samii, Madjid" sort="Samii, Madjid" uniqKey="Samii M" first="Madjid" last="Samii">Madjid Samii</name>
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<author><name sortKey="Sturm, Volker" sort="Sturm, Volker" uniqKey="Sturm V" first="Volker" last="Sturm">Volker Sturm</name>
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<author><name sortKey="Barnikol, Utako B" sort="Barnikol, Utako B" uniqKey="Barnikol U" first="Utako B" last="Barnikol">Utako B. Barnikol</name>
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<author><name sortKey="Auburger, Georg" sort="Auburger, Georg" uniqKey="Auburger G" first="Georg" last="Auburger">Georg Auburger</name>
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<author><name sortKey="Tass, Peter A" sort="Tass, Peter A" uniqKey="Tass P" first="Peter A" last="Tass">Peter A. Tass</name>
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<term>Female</term>
<term>Follow-Up Studies</term>
<term>Humans</term>
<term>Neurologic Examination</term>
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<term>Deep Brain Stimulation</term>
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<front><div type="abstract" xml:lang="en">This is a single case report of a patient with spinocerebellar ataxia type 2 (SCA2) and severe tremor. Whereas disease progression with prevailing ataxia and dysmetria was slow over the first symptomatic 6 years, 6 months prior to operation were characterized by the development of a severe, debilitating postural tremor rendering the patient unable to independently sit, stand, speak, or swallow. Deep brain stimulation (DBS) at a subthalamic-thalamic electrode position almost completely arrested her tremor. The patient regained the functional state prior to her rapid disease progression allowing a restricted range of daily activities. Her condition has remained approximately stable over the two postoperative years to date. In addition to the efficacy of DBS on cerebellar tremor, the results illustrate a remarkable improvement of the patient's general condition and independence.</div>
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