Bogacz J, Chouza C, Romero S, Bogacz A, Correa H, Barbeau A
Can J Neurol Sci. 1984 Nov;11(4 Suppl):565-9. doi: 10.1017/s0317167100035058.
Six patients with Friedreich's ataxia, 4 males and 2 females, their ages ranging from 13 to 33 years, were studied. The early manifestations started between age 7 and 13 with an evolution time between 6 and 20 years. Serial visual and brain stem auditory evoked potential recordings were made. A progressive increase in latency, reduction in amplitude and in latency inter-ocular difference of P100 were observed. The pattern of the reversal checker-board visual evoked potential was preserved. A disorganized BAEP pattern, a well defined potential I, a very small potential V and a delay in the interpeak latency were constant findings. The assumption is made of a progressive involvement of both visual and central auditory pathways. Pathophysiological mechanisms are discussed.
对6例弗里德赖希共济失调患者进行了研究,其中男性4例,女性2例,年龄在13至33岁之间。早期表现始于7至13岁,病程为6至20年。进行了系列视觉和脑干听觉诱发电位记录。观察到P100潜伏期逐渐延长、波幅降低以及两眼间潜伏期差异减小。反转棋盘格视觉诱发电位的模式得以保留。BAEP模式紊乱、I波明确、V波极小以及峰间潜伏期延迟是恒定的表现。推测视觉和中枢听觉通路均有进行性受累。并对病理生理机制进行了讨论。