A universal newborn hearing screening with hearing and deafness predisposing genes in 1234 newborn babies
- VernacularTitle:1234例新生儿听力与聋病易感基因联合筛查
- Author:
Li LI
;
Jian HE
;
Yufen GUO
;
Lan LAN
;
Yiming YUAN
;
Yazhen LIU
;
Hong ZHANG
;
Haina DING
;
Rongjun MAN
;
Jianqiang LI
;
Julan YANG
;
Dayong WANG
;
Hui GUO
;
Qiuju WANG
- Publication Type:Journal Article
- Keywords: Neonatal Screening; Infant; Preventive Health Services; Genes
- From: Chinese Archives of Otolaryngology-Head and Neck Surgery 2006;0(04):-
- CountryChina
- Language:Chinese
- Abstract: G heterozygote carriers.The carrying rate of deafness gene was 26‰(32/1234).In the 32 carriers,there are 5 babies showed 'refer' at the first step of hearing screening.In the 1234 babies,112 babies showed 'refer' at the first step of hearing screening.CONCLUSION Deafness gene screening can make up for the deficiencies of the universal newborn hearing screening,and should be used in this kind screening more widely.