Movement Disorders (revue)

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Topiramate therapy for paroxysmal kinesigenic choreoathetosis

Identifieur interne : 002105 ( Istex/Checkpoint ); précédent : 002104; suivant : 002106

Topiramate therapy for paroxysmal kinesigenic choreoathetosis

Auteurs : Yuan-Gui Huang [République populaire de Chine] ; Yun-Chun Chen [République populaire de Chine] ; Fang Du [République populaire de Chine] ; Rui Li [République populaire de Chine] ; Ge-Lin Xu [République populaire de Chine] ; Wen Jiang [République populaire de Chine] ; Jing Huang [République populaire de Chine]

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RBID : ISTEX:804AD4AFE2AAFFCBCA39215F747DB3FF8E32163A

English descriptors

Abstract

We observed the clinical efficacy of topiramate for paroxysmal kinesigenic choreoathetosis (PKC). Topiramate was administered as a monotherapy with titrated dosages to 8 patients with PKC. Target daily dose of topiramate was 100 to 200 mg; the follow‐up period ranged from 8 months to 2 years. All of the patients became attack‐free, and side effects were mild. The results show that topiramate is effective as a monotherapy for treating patients with PKC. The response to topiramate indicates that the disease may be caused by an ion channel defect. © 2004 Movement Disorder Society

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DOI: 10.1002/mds.20283


Affiliations:


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ISTEX:804AD4AFE2AAFFCBCA39215F747DB3FF8E32163A

Le document en format XML

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<div type="abstract" xml:lang="en">We observed the clinical efficacy of topiramate for paroxysmal kinesigenic choreoathetosis (PKC). Topiramate was administered as a monotherapy with titrated dosages to 8 patients with PKC. Target daily dose of topiramate was 100 to 200 mg; the follow‐up period ranged from 8 months to 2 years. All of the patients became attack‐free, and side effects were mild. The results show that topiramate is effective as a monotherapy for treating patients with PKC. The response to topiramate indicates that the disease may be caused by an ion channel defect. © 2004 Movement Disorder Society</div>
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