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在广泛开展新生儿听力筛查的基础上进行聋病基因同步筛查的可行性和实施方案。新生儿聋病易感基因筛查在新生儿出生时和出生后3 d内进行新生儿脐带血和足跟血采集来筛查聋病易感和常见基因,策略上亦包括普遍人群筛查和目标人群筛查。新生儿听力筛查的目标希望做到聋而不哑,而融入聋病易感基因筛查则可以做到在全社会范围内有效减少聋儿的出生,有效咨询耳聋基因的携带者,使他们孕育一个健康的新生儿。
Feasibility and implementation plan of synchronous screening of deafness genes based on the extensive screening of newborn hearing. Neonatal Deaf Disease Susceptibility Gene Screening Neonatal cord blood and heel blood samples are taken at birth and within 3 days of birth to screen susceptible and common genes for deafness. The strategy also includes general population screening and Target population screening. The goal of neonatal hearing screening hopes to be deaf and not dumb, and integration into deaf disease susceptibility genetic screening can effectively reduce the birth of deaf children in the whole society, and effectively consult deafness gene carriers so that they Nurture a healthy newborn.