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Research progress in pathogenic genes of hereditary non-syndromic mid-frequency deafness 被引量:8
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作者 Wenjun Xia Fei Liu Duan Ma 《Frontiers of Medicine》 SCIE CAS CSCD 2016年第2期137-142,共6页
Hearing impairment is considered as the most prevalent impairment worldwide. Almost 600 million people in the world suffer from mild or moderate hearing impairment, an estimated 10% of the human population. Genetic fa... Hearing impairment is considered as the most prevalent impairment worldwide. Almost 600 million people in the world suffer from mild or moderate hearing impairment, an estimated 10% of the human population. Genetic factors play an important role in the pathogenesis of this disorder. Hereditary hearing loss is divided into syndromic hearing loss (associated with other anomalies) and non-syndromic hearing loss (not associated with other anomalies). Approximately 80% of genetic deafness is non-syndromic. On the basis of the frequency of hearing loss, hereditary non-syndromic hearing loss can be divided into high-, mid-, low-, and total-frequency hearing loss. An audiometric finding of mid-frequency sensorineural hearing loss, or a "bowl-shaped" audiogram, is uncommon. Up to now, merely 7 loci have been linked to mid-frequency hearing loss. Only four genetic mid- frequency deafness genes, namely, DFNA10 (EYA4), DFNA8/12 (TECTA), DFNA13 (COLIIA2), DFNA44 (CCDC50), have been reported to date. This review summarizes the research progress of the four genes to draw attention to mid-frequency deafness genes. 展开更多
关键词 hereditary non-syndromic hearing loss mid-frequency hearing loss deafiaess genes
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中频感音神经性耳聋分子病因研究进展 被引量:2
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作者 李佳 高雪 徐金操 《中国听力语言康复科学杂志》 2017年第6期437-439,共3页
感音神经性耳聋根据受累频率不同分为低频、中频、高频和全频耳聋。其中,中频感音神经性耳聋是一种特殊类型,有其独特的病因。下一代基因测序技术出现以后,针对中频感音神经性耳聋的病因学研究取得了飞速进展。研究认为,遗传因素在中频... 感音神经性耳聋根据受累频率不同分为低频、中频、高频和全频耳聋。其中,中频感音神经性耳聋是一种特殊类型,有其独特的病因。下一代基因测序技术出现以后,针对中频感音神经性耳聋的病因学研究取得了飞速进展。研究认为,遗传因素在中频感音神经性耳聋的发生中发挥了重要作用。本文结合大量国内外文献对中频听力下降为主的感音神经性耳聋的病因学、临床表现、愈后及治疗方法进行系统综述,以期对临床中频感音神经性耳聋诊治提供帮助。 展开更多
关键词 中频感音神经性耳聋 遗传因素 病因学
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