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[运动神经元病中眼球运动障碍的分析]

[Analysis of oculomotor disorders in motor neuron disease].

作者信息

Saito S, Yamamoto H

出版信息

Rinsho Shinkeigaku. 1989 Aug;29(8):969-75.

PMID:2513155
Abstract

Oculomotor disorders have been considered to be one of the negative symptoms in motor neuron disease (MND). However, recently, ophthalmoplegia, abnormal Bell's phenomenon and disturbance of pursuit movement have been reported. We tried to evaluate 32 patients with MND (19 males and 13 females; age, 35 to 77 years; 52.4 +/- 10.1 years) by bedside examination and electro-oculography (EOG) using an eye tracking method. Twenty-three of them were classified as amyotrophic lateral sclerosis (ALS) and seven as bulbospinal muscular atrophy, and two were unclassified. One hundred healthy persons for bedside examination and twenty-two for EOG were investigated as controls. Findings by bedside examinations were as follows; 1) Slight limitations of upward only, up & downward and upward & horizontal gaze were observed in 5 cases (15.6%), 1 case (3.1%) and 1 case (3.1%), respectively. 2) Incomplete convergence was observed in 11 cases. (34.4%) 3) Horizontal gaze nystagmus was observed in 6 cases. (18.8%) 4) As regards the frequency of limitation of upward gaze and incomplete convergence, there were no statistically significant differences from those in controls. Electrooculographic results were: 1) square wave jerks (SWJs) were recorded in 3 cases. (9.4%) 2) Amplitude ratio of saccade was significantly higher in MND than that in controls with the risk less than 0.1%. 3) The degree of ocular dysmetria was significantly higher in MND than that in controls with the risk less than 0.5%. These abnormalities were not directly related to suffering period. Although the mechanism is not known, several reports of the effectiveness of thyrotropin releasing hormone (TRH) in ALS were recently published.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

动眼神经障碍一直被认为是运动神经元病(MND)的阴性症状之一。然而,最近有报告称出现了眼肌麻痹、异常贝尔现象和追踪运动障碍。我们试图通过床边检查和使用眼动追踪方法的眼电图(EOG)对32例MND患者(19例男性和13例女性;年龄35至77岁,平均52.4±10.1岁)进行评估。其中23例被归类为肌萎缩侧索硬化症(ALS),7例为延髓脊髓性肌萎缩症,2例未分类。选取100名健康人进行床边检查,22名进行EOG检查作为对照。床边检查结果如下:1)仅向上、向上和向下以及向上和水平注视有轻微受限的分别有5例(15.6%)、1例(3.1%)和1例(3.1%)。2)11例(34.4%)观察到不完全集合。3)6例(18.8%)观察到水平注视性眼球震颤。4)向上注视受限和不完全集合的频率与对照组相比无统计学显著差异。眼电图结果为:1)3例(9.4%)记录到方波急跳(SWJs)。2)MND患者扫视幅度比显著高于对照组,风险小于0.1%。3)MND患者眼球运动失调程度显著高于对照组,风险小于0.5%。这些异常与患病时长无直接关系。尽管其机制尚不清楚,但最近有几篇关于促甲状腺激素释放激素(TRH)对ALS有效的报道。(摘要截断于250字)

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