A Clinical Study of 2788 Newborns Screened for Hearing and Gene / 听力学及言语疾病杂志
Journal of Audiology and Speech Pathology
; (6)1998.
Article
in Zh
| WPRIM
| ID: wpr-533994
Responsible library:
WPRO
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.
Full text:
1
Index:
WPRIM
Language:
Zh
Journal:
Journal of Audiology and Speech Pathology
Year:
1998
Type:
Article