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Cochlear implants in genetic deafness 被引量:1

Cochlear implants in genetic deafness
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摘要 Genetic defects are one of the most important etiologies of severe to profound sensorineural hearing loss and play an important role in determining cochlear implantation outcomes.While the pathogenic mutation types of a number of deafness genes have been cloned,the pathogenesis mechanisms and their relationship to the outcomes of cochlear implantation remain a hot research area.The auditory performance is considered to be affected by the etiology of hearing loss and the number of surviving spiral ganglion cells,as well as others.Current research advances in cochlear implantation for hereditary deafness,especially the relationship among clinic-types,genotypes and outcomes of cochlear implantation,will be discussed in this review. Genetic defects are one of the most important etiologies of severe to profound sensorineural hearing loss and play an important role in determining cochlear implantation outcomes.While the pathogenic mutation types of a number of deafness genes have been cloned,the pathogenesis mechanisms and their relationship to the outcomes of cochlear implantation remain a hot research area.The auditory performance is considered to be affected by the etiology of hearing loss and the number of surviving spiral ganglion cells,as well as others.Current research advances in cochlear implantation for hereditary deafness,especially the relationship among clinic-types,genotypes and outcomes of cochlear implantation,will be discussed in this review.
作者 Xuezhong Liu
出处 《Journal of Otology》 2014年第4期156-162,共7页 中华耳科学杂志(英文版)
关键词 Connexin Cx26/Cx30 Usher syndrome Mitochondria genes Waardenburg syndrome Auditory neuropathy Connexin Cx26/Cx30 Usher syndrome Mitochondria genes Waardenburg syndrome Auditory neuropathy
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