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Novel heterozygous mutations in the otogelin-like (OTOGL) gene in a child with bilateral mild nonsyndromic sensorineural hearing loss.

Gene - 15 Jan 2022

Pan Chen, Li Jun, Wang Shixin, Shi Chen, Zhang Yunmei, Yu Yafeng

Abstract excerpt

Hearing loss is a common disease, of which genetic factors are the main cause. The incidence of mild or moderate postlingual deafness in children is not high, and the impact on life and learning is not as severe as that of prelingual deafness. This leads to insufficient attention to the disorder in the clinic. To date, only a few disease-causing genes have been reported. This report describe a case of novel...

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PMID: 34626719
DOI: 10.1016/j.gene.2021.146000

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