Hearing outcomes after cochlear implantation in two patients with ATP6V1B2-related deafness and onychodystrophyChamieh, Sarah (Avtor) Marzin, Pauline (Avtor) Achard, Sophie (Avtor) Blanc, Pierre (Avtor) Jonard, Laurence (Avtor) Battelino, Saba (Avtor) Trebušak Podkrajšek, Katarina (Avtor) Serey-Gaut, Margaux (Avtor) Marlin, Sandrine (Avtor) ATP6V1B2cochlear implantationDODdisorders of developmentsensorineural hearing losssyndromic hearing lossZimmerman-Laband syndromeThe gold standard recommendation for congenital sensorineural hearing loss (SNHL) care is cochlear implantation (CI). Adjusting for confounding factors such as developmental comorbidities is crucial when assessing expected outcomes of the procedure for the patients, their families, and their medical teams. We describe two clinical cases of the deafness and onychodystrophy (DOD) spectrum and the benefit of molecular diagnosis to underline the importance of genetic testing when evaluating potential CI outcomes in syndromic congenital SNHL.20262026-08-06 10:30:39Neznano31706UDK: 616.21ISSN pri članku: 1878-0849DOI: 10.1016/j.ejmg.2026.105090COBISS_ID: 285043459sl