Parving A, Bak-Pedersen K
Acta Otolaryngol. 1978 Mar-Apr;85(3-4):184-90. doi: 10.3109/00016487809111925.
The otological and audiological findings in 39 patients with sensorineural low frequency hearing loss are reported. This type of perceptive hearing loss is difficult to distinguish from the true conductive hearing losses due to the air conduction audiogram shape and the invalidity of bone conduction determinations showing a false "air-bone gap". This may lead to surgical treatment of a perceptive hearing loss, as reported in the four case histories. By various audiological tests, contradictory information may be obtained. In our material, Bing's test and absent acoustic reflexes indicated a conductive disorder in 25% of the ears. The final differentiation may require cochleography. The hearing loss may be diagnosed as Meniere's disease. In our material only 17% complained of tinnitus and no patients had vertigo. Consequently, we find sensorineural low frequency hearing loss to differ from Meniere's disease. Our material comprises different etiological types of perceptive low frequency hearing loss. On type was inherited as an autosomal dominant trait, another type due to cochlear malformation probably also inherited, and a third group showing diverse audiological results. When the diagnosis is established, the patients may be treated successfully by specially constructed hearing aids.
报告了39例感音神经性低频听力损失患者的耳科和听力学检查结果。由于气导听力图的形状以及骨导测定显示出假的“气骨导间距”而无效,这种类型的感音性听力损失很难与真正的传导性听力损失区分开来。正如四个病例报告中所述,这可能导致对感音性听力损失进行手术治疗。通过各种听力学测试,可能会获得相互矛盾的信息。在我们的研究对象中,宾氏试验和听觉反射缺失表明25%的耳朵存在传导性障碍。最终的鉴别可能需要进行耳蜗电图检查。这种听力损失可能被诊断为梅尼埃病。在我们的研究对象中,只有17%的患者抱怨有耳鸣,没有患者有眩晕症状。因此,我们发现感音神经性低频听力损失与梅尼埃病不同。我们的研究对象包括不同病因类型的感音性低频听力损失。一种类型是作为常染色体显性性状遗传的,另一种类型是由于耳蜗畸形可能也是遗传的,还有第三组显示出不同的听力学结果。当诊断确立后,患者可以通过特制的助听器得到成功治疗。