Abstract：Objective To carry out mutation analysis of deafness-associated genes for deaf newborns and their parents,and to estimate the recurrence risk for their parents to have deaf descendants. Methods Suspected cases of inherited deafness were identified by neonatal hearing screening and questionnaires. Genomic DNAs of suspected cases and their parents were extracted from their peripheral blood samples . Common deafness-associated genes （ i.e. GJB2,SLC26A4 and 12S rRNA genes） were amplified by polymerase chain reaction（PCR）,and those PCR products were sequenced for the mutation analysis. Results From 2013 to 2016, 193 cases of deafness were found in neonatal hearing screening,29 cases of suspected as hereditary deafness were screened,and 17 out of 29 cases were found to have mutations in deafness-associated genes （detection rate：58.62%）. GJB2 homozygous mutations were identified in two cases and their parents,and the recurrence risk to have deaf descendants was 100%. Four cases of suspected hereditary deafness had GJB2 homozygous mutations,and their parents were both GJB2 mutation carriers. There was one case with SLC26A4 homozygous mutations,and their parents were both SLC26A4 mutation carrier. Two cases were detected to have GJB2 V371 homozygous mutations,and their parents were both GJB2 V371 mutation carriers. For those seven parents carrying deafness-associated mutations above,the recurrence risk of deafness for their descendants was 25%. Conclusion In addition to hearing screening,the genetic diagnosis of deafness-associated genes is helpful to clarify the cause of suspected neonatal hereditary deafness,and can provide objective reproductive counseling and guidance for those deaf parents or parents with deaf children.
YOSHIKAWA S,KAWANO A,HAYASHI C,et al. The clinical features of patients with the homozygous 235delC and the compound-heterozygous Y136X/G45E of the GJB2 mutations （Connexin 26） in cochlear implant recipients[J]. Auris Nasus Larynx,2011,38（4）：444-449.
