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[脊髓小脑遗传性变性累及中的早期听觉诱发电位]

[Early auditory evoked potentials in spinocerebellar heredodegenerative involvement].

作者信息

Belkahia A, Ben H'mida M, Ben Jelloul N, Gassab A, Chakroun A

出版信息

Ann Otolaryngol Chir Cervicofac. 1985;102(2):97-103.

PMID:4004026
Abstract

Results of early auditory evoked potentials, recorded during exploration of spinocerebellar heredodegenerative lesions (21 cases of Friedreich's disease, 8 cases of Pierre-Marie's disease and 3 cases of Strumpell-Lorraine disease), are analyzed. Tracings showed alteration of auditory BER whereas tonal audiometry was normal. Analysis of BER demonstrated lengthening of the latency periods, a rise in thresholds without latency period increases and a tracing that was sometimes flat or with waves that were difficult to recognize.

摘要

分析了在探索脊髓小脑遗传性退行性病变(21例弗里德赖希共济失调、8例皮埃尔 - 玛丽病和3例施特吕姆佩尔 - 洛林病)期间记录的早期听觉诱发电位结果。描记图显示听觉脑干反应(BER)改变,而纯音听力测定正常。对BER的分析表明潜伏期延长、阈值升高但潜伏期无增加,并且描记图有时呈平坦状或有难以识别的波。

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