摘要
新生儿听力筛查可以早期发现听力障碍儿童,并对其进行诊断、早期干预,从而达到早期康复的目的。耳聋基因筛查可以预警迟发性耳聋以及药物敏感性耳聋。本文对我国不同地区新生儿听力和耳聋基因联合筛查的应用进行综述。
Neonatal hearing screening can be found in the early detection of hearing impaired children,and its diagnosis,early intervention,so as to achieve the purpose of early rehabilitation. Deafness gene screening can be early warning of delayed deafness and drug sensitivity of hearing loss. This paper summarizes the application of combined screening of neonatal hearing and deafness genes in different regions of China.
出处
《中国优生与遗传杂志》
2016年第7期11-12,共2页
Chinese Journal of Birth Health & Heredity
关键词
不同地区
听力损失
基因
联合筛查
Different regions
Hearing loss
Gene
Combined screening
