更全面的听力筛查策略——新生儿听力与聋病基因联合筛查  

More universal hearing screening:combination screening of hearing and gene of newborn

作　　者：马秀岚[1] 张东红[1] 

机构地区：[1]中国医科大学附属盛京医院耳科,辽宁省儿童听力障碍诊治中心,辽宁沈阳110004

出　　处：《中国医学文摘（耳鼻咽喉科学）》2015年第4期199-201,共3页Chinese Medical Digest(Otorhinolaryngology)

摘　　要：在新生儿普遍听力筛查的基础上,同步进行聋病基因筛查,可以相互补充单一筛查时的局限性,既可以第一时间发现先天性听力损伤并及早干预和治疗,又可以第一时间确定迟发性遗传性听力障碍高危人群,通过采取措施积极应对,减少或延迟遗传性听力障碍的发生,不失为更全面高效的听力筛查策略。The synchronized deafness genetic screening on the basis of common newborn hearing screening can break their respective limits. Early intervention and treatment could be given,if congenital hearing loss can be found earlier. It also can determine risk populations with delayed hereditary hearing impairment as early as possible. The combined screening is a more comprehensive and efficient hearing screening strategy,which can reduce or delay the occurrence of hereditary hearing impairment by taking active measures.

关 键 词：新生儿筛查 听力 基因 联合筛查 

分 类 号：R722.19[医药卫生—儿科]