Molecular analysis by means of a deafness gene panel [WESHL panel v2.0] identified a heterozygous variant in the CHD7 [NM_017780.4]: c.6193C>T p.[Arg2065Cys] and the myosin IIIA [MYO3A] [NM_017433.5]: c.3133G>T p.[Val1045Leu] gene, both classified as class 3 variants or variants of unknown significance. Here, CHD7 is linked to deafness.