人类耳蜗突触病。证据回顾和未来发展方向

G. Panagiotopoulos
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引用次数: 0

摘要

耳蜗突触病,是一种损伤位于ihc和i型传入听神经纤维之间的突触水平的情况。这些突触的功能被破坏,要么不能重建,要么不能重建,从而导致各种信号编码缺陷和听力障碍。耳蜗突触病可广泛存在于毛细胞群完整、听音图相对“正常”的耳朵中,是“隐性”听力损失的主要原因。本研究综述了隐蔽性听力损失的主要机制,强调了人类耳蜗突触病的正确诊断的未来方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cochlear Synaptopathy in Humans. Review of the Evidence and Future Directions
Cochlear synapthopathy, is a condition where the damage is located at the level of the synapses between IHCs and type-I afferent auditory nerve fibres. The disrupted function of these synapses, either can or can’t be re-established, thus resulting in various signal coding deficits and hearing impairment. Cochlear synaptopathy can be widely present in ears with intact hair cell populations and relatively ‘normal’ audiograms, representing the major cause of “hidden” hearing loss. The present study reviews the major mechanisms involved in hidden hearing loss, emphasizing on future directions regarding appropriate diagnosis of cochlear synaptopathy in humans.
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