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腿部刻板综合征:现象学与流行率。

Leg stereotypy syndrome: phenomenology and prevalence.

机构信息

Department of Neurology, Parkinson's Disease Center and Movement Disorders Clinic, Baylor College of Medicine, Houston, Texas, USA.

出版信息

J Neurol Neurosurg Psychiatry. 2018 Jul;89(7):692-695. doi: 10.1136/jnnp-2017-317057. Epub 2018 Jan 13.

Abstract

OBJECTIVES

To describe the phenomenology and prevalence of leg stereotypy syndrome (LSS), characterised chiefly by repetitive, rhythmical, stereotypic leg movement, especially when sitting.

METHODS

We sought to characterise LSS in two groups of subjects: (1) general population (GP) group, defined as individuals accompanying patients during their visits to Baylor College of Medicine Parkinson's Disease Center and Movement Disorders Clinic who are not genetically related to the patients; and (2) movement disorders (MD) group, composed of consecutive patients with diagnoses of restless legs syndrome, Parkinson's disease, Tourette syndrome and tardive dyskinesia.

RESULTS

There were 92 participants enrolled in this study; 7% of 57 individuals in the GP group and 17% of those in the MD group met the diagnostic criteria for LSS. The mean age of individuals with LSS was 44.5 (±11.9) years and mean age at onset of LSS was 17.5 (±5.7) years. In half of the individuals, the 'shaking' involved predominantly one leg. All had a positive family history of similar disorder and none had diurnal variation. The seven-item Leg Stereotypy Syndrome Questionnaire was developed as a screening tool to aid in differentiating LSS from other movement disorders.

CONCLUSIONS

LSS is a common condition, occurring in up to 7% of otherwise healthy individuals, and it is even more common in patients with hyperkinetic movement disorders. Although it phenomenologically may overlap with other stereotypic disorders, we argue that it is a distinct, familial, neurological syndrome.

摘要

目的

描述腿部刻板综合征(LSS)的现象学和流行情况,其主要特征是重复性、节律性、刻板性腿部运动,尤其是在坐着时。

方法

我们试图在两组受试者中描述 LSS:(1)普通人群(GP)组,定义为在贝勒医学院帕金森病中心和运动障碍诊所就诊的患者的家属,他们与患者没有遗传关系;(2)运动障碍(MD)组,由连续诊断为不宁腿综合征、帕金森病、图雷特综合征和迟发性运动障碍的患者组成。

结果

本研究共纳入 92 名参与者;GP 组 57 人中的 7%和 MD 组中的 17%符合 LSS 的诊断标准。患有 LSS 的个体的平均年龄为 44.5(±11.9)岁,LSS 的平均发病年龄为 17.5(±5.7)岁。在一半的个体中,“抖动”主要涉及一条腿。所有人都有类似疾病的阳性家族史,且无昼夜变化。开发了七项腿部刻板综合征问卷作为一种筛查工具,以帮助区分 LSS 与其他运动障碍。

结论

LSS 是一种常见的疾病,在 7%的健康个体中发生,在患有多动性运动障碍的患者中更为常见。尽管它在表现上可能与其他刻板障碍重叠,但我们认为它是一种独特的、家族性的、神经科的综合征。

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