Suppr超能文献

原发性抽动障碍伴发肌张力障碍的临床综合征:一项大型临床系列研究及文献复习

The clinical syndrome of primary tic disorder associated with dystonia: a large clinical series and a review of the literature.

机构信息

Sobell Department of Motor Neuroscience and Movement Disorders, Institute of Neurology, UCL, Queen Square, London, United Kingdom.

出版信息

Mov Disord. 2011 Mar;26(4):679-84. doi: 10.1002/mds.23484. Epub 2011 Jan 12.

Abstract

BACKGROUND

The co-occurrence of tics and dystonia as an idiopathic condition has only rarely been reported. We report a series of patients with tics and persistent dystonia, with the aim of determining the prevalence and clinical characteristics of this syndrome.

METHODS

Analysis of clinical database of patients with tic disorders.

RESULTS

From our database of 224 patients with tics, 20 had co-occurrence of tics and dystonia as a primary disorder. Six patients had Tourette's syndrome, and 2 had idiopathic chronic motor/phonic tics. Twelve of the 20 had adult onset of tics (9 with motor/phonic tics and 3 with motor tics). Dystonia was focal in 12 patients (cervical most common) and segmental in 8. A sensory geste was present in 8. Mean age of tic onset and dystonia was 28.3 ± 19.7 and 40.5 ± 15.3 years, respectively. Tics preceded dystonia in 12, dystonia preceded tics in 4, and 1 patient had simultaneous onset of tics and dystonia. In 3 patients, symptoms' sequence could not be determined. Only 8 patients required treatment for their tics. Botulinum toxin was the mainstay of dystonia treatment (16 patients), whereas 6 received trihexyphenidyl. Six patients each had depression and obsessive compulsive symptoms, and 5 had attention-deficit and hyperactivity disorder.

DISCUSSION

We have further characterized the syndrome of a primary condition of tics associated with persistent focal/segmental dystonia. Apart from the presence of dystonia, our data suggest that these patients are differentiated from pure tic disorders by a later age of onset, lesser severity of tics, and lower frequency of associated features.

摘要

背景

抽动和肌张力障碍同时出现作为一种特发性疾病的情况很少有报道。我们报告了一系列抽动伴持续性肌张力障碍的患者,旨在确定该综合征的患病率和临床特征。

方法

分析抽动障碍患者的临床数据库。

结果

从我们的 224 例抽动患者的数据库中,有 20 例抽动和肌张力障碍同时出现作为原发性疾病。6 例患者患有妥瑞氏综合征,2 例患有特发性慢性运动/发音抽动。20 例患者中有 12 例(9 例为运动/发音抽动,3 例为运动性抽动)为成人起病。12 例患者的肌张力障碍为局灶性(最常见于颈部),8 例为节段性。8 例存在感觉性动作。抽动的发病年龄和肌张力障碍的发病年龄分别为 28.3±19.7 岁和 40.5±15.3 岁。12 例患者中抽动先于肌张力障碍,4 例患者中肌张力障碍先于抽动,1 例患者同时出现抽动和肌张力障碍。在 3 例患者中,无法确定症状的顺序。只有 8 例患者需要治疗他们的抽动。肉毒杆菌毒素是肌张力障碍治疗的主要方法(16 例),而 6 例患者接受了三己酚。6 例患者各有抑郁和强迫症症状,5 例患者有注意力缺陷和多动障碍。

讨论

我们进一步描述了原发性抽动伴持续性局灶性/节段性肌张力障碍的综合征。除了肌张力障碍的存在外,我们的数据表明,这些患者与单纯抽动障碍的区别在于发病年龄较晚、抽动症状较轻、相关特征的频率较低。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验