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弗里德赖希共济失调中的动眼神经异常。

Oculomotor abnormalities in Friedreich's ataxia.

作者信息

Kirkham T H, Guitton D, Katsarkas A, Kline L B, Andermann E

出版信息

Can J Neurol Sci. 1979 May;6(2):167-72. doi: 10.1017/s0317167100119584.

Abstract

A clinical neuro-ophthalmological and electro-oculographic study was made on fourteen patients with Friedreich's ataxia. None had evidence of optic nerve dysfunction. No patient complained of oscillopsia although all had ocular motor deficits of varying degrees, which appeared to be related to the severity of the general manifestations of the disease. The defects comprised square wave jerks, jerky pursuit with inability to maintain eccentric gaze resulting in gaze paretic nystagmus and rebound nystagmus. There was failure to suppress by fixation the vestibulo-ocular reflex. The slow phase velocity of caloric nystagmus was always of reduced velocity. There was inability to augment the slow phase velocity of optokinetic nystagmus with increasing stimulus velocity. Abnormalities of the saccadic system were manifest particularly as hypermetria. These signs in combination are suggestive of disease involving the cerebellar flocculus and vermis or their brain stem connections. No abnormalities were found in 17 parents or siblings.

摘要

对14例弗里德赖希共济失调患者进行了临床神经眼科和眼电图研究。无一例有视神经功能障碍的证据。尽管所有患者都有不同程度的眼球运动缺陷,且这些缺陷似乎与疾病总体表现的严重程度相关,但无一例患者主诉视振荡。这些缺陷包括方波急跳、急动性跟踪障碍,无法维持偏心注视,导致注视性麻痹性眼球震颤和反弹眼球震颤。注视不能抑制前庭眼反射。冷热试验性眼球震颤的慢相速度总是降低的。随着刺激速度增加,视动性眼球震颤的慢相速度无法增加。扫视系统异常尤其表现为辨距过度。这些体征综合起来提示疾病累及小脑绒球和蚓部或其脑干连接。17名父母或兄弟姐妹未发现异常。

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