摘要
目的探讨听神经病的病损部位及发病机制。方法常规检测听神经病患者(10例,20耳)和正常听力者(10例,20耳)的纯音听力及DPOAE,并对结果进行比较和统计学分析。结果听神经病组20耳中18耳纯音测听呈低频下降型听力损失,另2耳呈鞍型听力曲线,低频(250、500、1000Hz)听力损失一般大于40dB。畸变产物耳声发射均可引出,各频率耳声发射幅值与正常对照组差异无统计学意义,纯音听力与相应频率耳声发射出现矛盾。结论听神经病的病损部位可能位于耳蜗传入通路,神经冲动非同步化或同步化受损是听神经病的发病机制之一。
Objetive To investigate and analyze the site of lesion and the macbanism of auditory neuropathy. Methods 10 patients(20 ears)with auditory neuropathy(AN) and 10 normal hearing youth(20 ears)were of audiological battery assessed with routine pure tone audiometry and distortion product otoacoustic emission. Data of the two groups were compared and analyzed statistically. Results Pure tone audiograms in 18 ears of AN group showed low - frequency hearing loss, while the other 2 showed a saddle - like threshold curve. The hearing loss at low frequency( 250,500,1 000 Hz) was more than 40 dB in most ears. Distortion product otoacoustic emission responses were present in all eases. The average amplitude at each frequency exhibited no significant difference compared with control group. Conclusion The site of lesion of auditory neuropathy may be in the cochlear afferent pathway. The asynchronization of the cochlear afferent nerve fibers may be responsible for auditory neuropathy, thus causing the contradiction.
出处
《听力学及言语疾病杂志》
CAS
CSCD
2007年第2期98-100,共3页
Journal of Audiology and Speech Pathology
关键词
听神经病
感音神经性聋
畸变产物耳声发射
Auditory neuropathy
Hearing loss, neurosensory
Distortion product otoacoustic emission