伴有保留的耳蜗微音和继发性耳声发射丧失的听神经病变。

P Deltenre, A L Mansbach, C Bozet, F Christiaens, P Barthelemy, D Paulissen, T Renglet
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引用次数: 135

摘要

听神经病被定义为缺乏或严重扭曲的听脑干反应,保留耳声发射和耳蜗微音。这个实体可以在各种情况下找到,包括不会说话的儿童。成人患者报告的一个几乎普遍的特征是传统助听器的无效。因此,对语言前病例的适当管理仍然是一个悬而未决的问题。本文描述了两名学龄前儿童的随访数据显示选择性耳声发射丧失,而耳蜗微音仍然保留。其中一名患者在失去耳声发射后立即进行了助听器安装,结果证明是成功的。这些发现对该病症的操作定义具有重要意义,因为必须准备好遇到没有耳声发射的病例。目前的数据还表明,传统的放大可以使语前听神经病变病例受益,至少一旦他们失去了耳声发射。
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Auditory neuropathy with preserved cochlear microphonics and secondary loss of otoacoustic emissions.

Auditory neuropathy is defined as absent or severely distorted auditory brainstem responses with preserved otoacoustic emissions and cochlear microphonics. This entity can be found in various circumstances including pre-lingual children. An almost universal characteristic reported from adult patients is the ineffectiveness of traditional hearing aids. Adequate management of pre-lingual cases therefore remains an open problem. This paper describes two pre-lingual children whose follow-up data demonstrated a selective loss of the otoacoustic emissions, whereas the cochlear microphonics remained preserved. In one of the patients, hearing aid fitting as soon as she lost her otoacoustic emissions proved successful. These findings have important implications for the operational definition of the condition, since one must be prepared to encounter cases with absent otoacoustic emissions. The present data also demonstrate that conventional amplification can benefit pre-lingual auditory neuropathy cases, at least once they have lost their otoacoustic emissions.

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