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多巴反应性肌张力障碍

Dopa-responsive dystonia.

作者信息

Nygaard T G, Marsden C D, Duvoisin R C

机构信息

Department of Neurology, UMDNJ-Robert Wood Johnson Medical School, New Brunswick.

出版信息

Adv Neurol. 1988;50:377-84.

PMID:3041760
Abstract

DRD is a distinctive clinical entity and an unexpectedly common subgroup of torsion dystonia. Diurnal fluctuation is often but not always present and does not reliably distinguish the disorder from ITD. DRD must be considered in the differential diagnosis of the child or adolescent presenting with a dystonic gait disorder, diplegic cerebral palsy, sporadic spastic paraplegia, ataxic syndromes, and juvenile parkinsonism. The response to L-DOPA is so dramatic and occurs so quickly that a diagnostic therapeutic trial should be undertaken in all patients presenting with these syndromes.

摘要

多巴反应性肌张力障碍是一种独特的临床实体,是扭转性肌张力障碍中意外常见的一个亚组。日间波动常常存在,但并非总是如此,且不能可靠地将该疾病与特发性扭转性肌张力障碍区分开来。对于出现肌张力障碍性步态障碍、双侧瘫脑瘫、散发性痉挛性截瘫、共济失调综合征和青少年帕金森病的儿童或青少年进行鉴别诊断时,必须考虑到多巴反应性肌张力障碍。对左旋多巴的反应非常显著且起效迅速,因此对于所有出现这些综合征的患者都应进行诊断性治疗试验。

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