Preimplantation genetic testing for hereditary hearing loss in Chinese population.
Qingling BiShasha HuangHui WangXue GaoMinyue MaMingyu HanSijia LuDongyang KangAida NourbakhshDenise YanSusan BlantonXuezhong LiuYongyi YuanYuanqing YaoPu DaiPublished in: Journal of assisted reproduction and genetics (2023)
In both the HL population and in hearing individuals at risk of giving birth to offspring with HL in China, there is a practical need for PGT. The whole genome amplification combined with NGS can simplify the PGT process, and the efficiency of PGT process can be improved by establishing a universal SNP bank of common disease-causing gene in particular regions and nationalities. This PGT procedure was demonstrated to be effective and lead to satisfactory clinical outcomes.