Newborn Screening of Genetic Mutations in Common Deafness Genes With Bloodspot-Based Gene Chip Array

Purpose This study screens for deafness gene mutations in newborns in the Northwest China population. Method The 9 sites of 4 common deafness genes (GJB2, GJB3, SLC26A 4, and mt 12S rRNA) were detected by bloodspot-based gene chip array in 2,500 newborns. Results We detected mutations of the 4 genes in 101 (4.04%) newborns; particularly, 0.20% detected the double mutations. In the Hui population, 4.58% of the newborns tested positive for mutations, whereas 4.01% of Han newborns tested positive for mutations. The detective rates are as follows: 1.44% for GJB2 235delC, 1.08% for SLC26A4 IVS7-2A>G, 0.48% for GJB2 299_300delAT, 0.28% for SLC26A4 2168A>G, 0.2% for mt 12S rRNA 1555A>G, and 0.16% for GJB3 538C>T. The 31.25% (5/16) of infants with GJB2 235delC, 50% (3/6) with GJB2 299_300delAT, and 25% (3/12) with SLC26A4 IVS7-2A>G showed abnormal hearing when tested; only 1 double mutation case received the hearing test, and this infant showed abnormality in both ears on the hearing test. Conclusions High mutati...