OCULOMOTOR ABNORMALITIES IN FRIEDREICHS ATAXIA

被引:39
作者
KIRKHAM, TH
GUITTON, D
KATSARKAS, A
KLINE, LB
ANDERMANN, E
机构
[1] MCGILL UNIV, DEPT NEUROL, MONTREAL H3C 3G1, QUEBEC, CANADA
[2] MCGILL UNIV, DEPT OTOLARYNGOL, MONTREAL H3C 3G1, QUEBEC, CANADA
[3] MCGILL UNIV, DEPT NEUROSURG, MONTREAL H3C 3G1, QUEBEC, CANADA
[4] MCGILL UNIV, DEPT OPTHALMOL, MONTREAL H3C 3G1, QUEBEC, CANADA
[5] MCGILL UNIV, DEPT NEUROGENET, MONTREAL H3C 3G1, QUEBEC, CANADA
[6] CLIN RES INST MONTREAL, MONTREAL H2W 1R7, QUEBEC, CANADA
[7] ROYAL VICTORIA HOSP, MONTREAL H3A 1A1, QUEBEC, CANADA
关键词
D O I
10.1017/S0317167100119584
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
A clinical neuro-opthalmo-logical 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 vestíbulo-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 cere be I lar flocculus and vermis or their brain stem connections. No abnormalities were found in 17 parents or siblings. © 1979, Canadian Neurological Sciences Federation. All rights reserved.
引用
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页码:167 / 172
页数:6
相关论文
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