In the group of patients with simultaneous vision and hearing impairment (14 individuals), the most frequent pathogenic variants in the USH2A gene were the previously described LoF-variants c.11864G>A (p.(Trp3955*)) (variant frequency 35.7%), c.8682-9A>G (17.8%), and c.9424G>T (p.(Gly3142*)) (7.1%). The gene discussed is USH2A; the disease is hearing loss disorder.