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伴发声的阵发性肌阵挛性肌张力障碍:新的疾病实体还是既往综合征的变异型?

Paroxysmal myoclonic dystonia with vocalisations: new entity or variant of preexisting syndromes?

作者信息

Feinberg T E, Shapiro A K, Shapiro E

出版信息

J Neurol Neurosurg Psychiatry. 1986 Jan;49(1):52-7. doi: 10.1136/jnnp.49.1.52.

Abstract

From among 1377 patients with movement disorders, four patients had an unusual movement disorder characterised by paroxysmal bursts of involuntary, regular, repetitive, rhythmic, bilateral, coordinated, simultaneous, stereotypic myoclonus and vocalisations, often associated with tonic symptoms, interference with voluntary functioning, presence of hyperactivity, attention and learning disabilities, and resistance to treatment with haloperidol and other drugs. This symptom complex may represent a new disease entity, referred to here as paroxysmal myoclonic dystonia with vocalisations or a variant or combination of other movement disorders such as Gilles de la Tourette, myoclonic, or dystonic syndromes.

摘要

在1377例运动障碍患者中,有4例患有一种不寻常的运动障碍,其特征为阵发性突发的不自主、规则、重复、有节奏、双侧、协调、同步、刻板的肌阵挛和发声,常伴有强直症状,干扰自主功能,存在多动、注意力和学习障碍,且对氟哌啶醇和其他药物治疗有抵抗性。这种症状复合体可能代表一种新的疾病实体,在此称为伴发声的阵发性肌阵挛性肌张力障碍,或其他运动障碍如吉兰-巴雷综合征、肌阵挛或肌张力障碍综合征的变体或组合。

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