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感音神经性听力障碍可采取以下措施加以预防Sensorineural hearing impairment can be prevented by

耳蜗畸形是先天性感音性聋的常见病因。Cochlear malformation is the common reason for congenital sensorineural hearing loss.

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下面是一个来自有知觉神经性失聪成员的家庭之家族系谱。Here is a pedigree from a family in which sensorineural deafness is present in some members.

根据类型又可分为传导性耳聋和感音神经性耳聋。According to types of deafness can be divided into conductive and sensorineural hearing loss.

儿童先天性感音神经性聋的早期干预非常重要。Early interventions are of great importance to children with congenital sensorineural deafness.

目的探讨感觉神经性耳聋与航空航天飞行的关系。Objective To probe the relations between sensorineural deafness and flying in aviation or space.

出现了一大批的原因，可分为传导性和感音神经性。It occurs for a large number of reasons, which can be categorised into conductive and sensorineural.

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感音神经性听力障碍是内耳道的问题，偶尔是听力神经上的问题。Sensorineural hearing impairment is a problem with the inner ear, or, occasionally with the hearing nerve.

治疗中、重度感音神经性耳聋，通常采用选配合适的助听器来恢复其听觉功能。The treatment of moderate and severe sensorineural hearing loss, usually by matching the appropriate hearing aids to restore its function.

感音神经性听力障碍通常是由于过量的噪音、衰老和脑膜炎、麻疹风疹和流行性腮腺炎等传染病所造成的。Sensorineural hearing impairment is commonly due to excessive noise, ageing and infectious diseases such as meningitis, measles rubella and mumps.

方法对93例感音性耳聋患者均采用颞骨轴位高分辨率CT螺旋扫描及内耳三维重建。Methods Axial high-resolution temporal bone CT and three-dimensional reconstruction of inner ear were performed in 93 patients with sensorineural hearing loss.

目的对重度感音神经性耳聋患儿行多道人工耳蜗植入术的相关护理问题进行探讨。Objective To discuss the nursing relevant question during transplanting multi-channel artificial cochlea for children with profound sensorineural hearing loss.

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目的报道一个进展缓慢的显性遗传性肩肱型脊髓性肌萎缩家系，探讨其临床特点和诊断规律。Objective Scapulohumeral type spinal muscular atrophy is a rare disorder. We report a new family with ophthalmoplegia , dropped head syndrome and sensorineural deafness.

结论感音神经性聋患者耳蜗或听觉传导通路的受损程度对穴位按摩疗效具有显著的影响。Conclusion The impairment degree of cochlea or auditory transduction pathway in sensorineural deafness patients has significant influence on the curative effect of point massage.

建议将此突变位点检测运用于遗传咨询、产前诊断、新生儿和不明原因感音神经性聋患者的基因筛查中。It is suggested to utilize this detection for genetic counseling, prenatal diagnosis, and the genetic screening of neonates and the sensorineural hearing loss with unknown reason.

毛细胞在体内、体外由于强声、耳毒性药物、老年化、外伤和各种疾病等造成的损伤，是感音神经性聋和平衡障碍的主要病理基础。The trauma of hair cells caused by strong sound, drug, aging, injury and various diseases in vitro and in vivo is sensorineural deafness and equilibrium problems' pathological base.

大部分听神经瘤的患者，常以单侧渐进性感觉神经性听力障碍及耳鸣表现，而少有以急性眩晕为表现症状。The most common early symptoms of acoustic neuroma are unilateral progressive sensorineural hearing impairment and tinnitus. Acoustic neuroma presenting as acute vertigo is less often.

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结论突发性耳聋患者发病后尽早开始包括地塞米松在内的药物治疗并辅助高压氧进行综合治疗有助于提高疗效和痊愈率。Conclusion Early drug treatment plus glucocorticosteroid and hyperbaric oxygen adjuvants would add the rates of effectiveness and cure in patients with sudden sensorineural hearing loss.

桥小脑角和前庭脂肪瘤是非常少见的，任何桥小脑角区或前庭区肿块都可以导致病人出现感音性听力丧失，就像本例一样。Cerebellopontine angle lipomas and vestibular lipomas are rare lesions. Any cerebellopontine angle or vestibular mass can cause a patient to present with sensorineural hearing loss, as in this case.