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This case report discusses a 10-year-old girl with bilateral sensorineural hearing loss (SNHL) linked to a heterozygous missense variant in the MYH7B gene. The report highlights the genetic basis of congenital SNHL, the role of whole exome sequencing in diagnosis, and the specific auditory dysfunction associated with MYH7B mutations. It emphasizes the importance of ongoing multidisciplinary care for affected individuals and the need for further research into gene-disease associations.

Author

International Journal of Innovative Science and Research Technology

Language

EN