Movement Disorders (revue)

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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 : 003A75

Subthalamic‐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 :

RBID : ISTEX:B79BA13EC8F75FDB2547F5F9F6AED56023BA7AD7

English descriptors

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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ISTEX:B79BA13EC8F75FDB2547F5F9F6AED56023BA7AD7

Le document en format XML

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<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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<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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