A Clinical Study of 2788 Newborns Screened for Hearing and Gene
- VernacularTitle:新生儿听力与聋病易感基因联合筛查的临床研究
- Author:
Shujun HU
;
Jianqiang LI
;
Peng ZHANG
;
Lan LAN
;
Jin ZHENG
;
La LI
;
Jie SONG
;
Dayong WANG
;
Hongxia TIAN
;
Haila DING
;
Songchuan WANG
;
Qiuju WANG
- Publication Type:Journal Article
- Keywords:
Newborn;
Hearing screening;
Genes screening;
Mutation
- From:
Journal of Audiology and Speech Pathology
1998;0(03):-
- CountryChina
- Language:Chinese
-
Abstract:
G mutation were intervened and avoided the occurrence of deafness,1 babies with 235delC homozygote was confirmed severe sensorineural hearing loss in the hearing screening.Conclusion Newborn gene screening make up the defects of missed diagnosis in simple hearing screening in finding the newborn babies with late-onset deafness or the high risk as well as the pathogenic carriers.So the hearing and gene screening were necessary in the current situation,and this screening strategy would be developed further in Henan province.
