Cochlear Nerve Hypoplasia: Audiological Characteristics in Children and Adults

B. Cinar, E. Tahir, Merve Ozbal Batuk, M. Yaralı, G. Sennaroğlu, L. Sennaroğlu
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引用次数: 2

Abstract

Background: Cochlear nerve deficiency is a general term used to describe both cochlear nerve hypoplasia (CNH) and cochlear nerve aplasia. Although these two conditions can have similar results on audiological evaluation, CNH yields more variation in audiological tests. Objectives: To describe the audiological characteristics of the CNH cases in our series in relation to radiological findings. Methods: We reviewed the medical charts, audiological findings, and radiological findings on cases with CNH. We included cases with CNH in one ear or both ears. Out of 90 subjects with CNH, we included a total of 40 individuals (21 women and 19 men; 49 ears) in the current study. We reviewed and analyzed the participants’ audiological test results according to the radiological findings. Results: Cases with CNH showed variations according to the cochlear structure. There were 13 normal cochleae, 4 with incomplete partition type I, and 32 with cochlear hypoplasia. The accompanying cochlear apertures also showed variation: 17 were normal, 28 stenotic, and 4 aplastic cochlear apertures. The subjects displayed hearing loss ranging from moderate to profound; furthermore, 4 subjects had no response to sound whatsoever. The degree of hearing loss was not statistically significantly different with regard to the presence or absence of cochlear malformation with CNH (p > 0.005). We observed both sensorineural hearing loss and mixed-type hearing loss among the CNH cases. Conclusions: CNH is the presence of a cochlear nerve that is smaller in diameter than the facial nerve. It can be accompanied with other associated inner ear malformations of different degrees of severity. We observed degrees of hearing loss ranging from moderate to profound.
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耳蜗神经发育不全:儿童和成人的听力学特征
背景:耳蜗神经缺损是耳蜗神经发育不全(CNH)和耳蜗神经发育不全的总称。虽然这两种情况在听力学评估中有相似的结果,但CNH在听力学测试中产生更多的差异。目的:描述本系列CNH病例的听力学特征与影像学表现的关系。方法:我们回顾了CNH病例的医学图表、听力学表现和影像学表现。我们纳入了单耳或双耳CNH病例。在90名CNH患者中,我们共纳入了40名个体(21名女性和19名男性;在当前的研究中。我们根据放射学结果回顾和分析了参与者的听力学测试结果。结果:CNH病例表现出不同耳蜗结构的差异。正常耳蜗13例,ⅰ型不完全分割耳蜗4例,耳蜗发育不全32例。伴随的耳蜗孔也有差异:17个正常,28个狭窄,4个再生耳蜗孔。受试者表现出中度到重度的听力损失;此外,4名受试者对声音没有任何反应。CNH患者的听力损失程度与是否存在耳蜗畸形差异无统计学意义(p < 0.05)。我们在CNH病例中观察到感觉神经性听力损失和混合型听力损失。结论:CNH是指耳蜗神经直径小于面神经。它可以伴随其他相关的内耳畸形不同程度的严重程度。我们观察到听力损失的程度从中度到重度不等。
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