What is the current medical evidence concerning prelingual hearing loss associated with POU3F4 and OPA1 gene variants?
Abstract
POU3F4 and OPA1 gene variants are associated with prelingual hearing loss, where POU3F4 relates to X-linked forms with structural ear abnormalities, while OPA1 variants improve cochlear implant outcomes for certain patients.
Fields of Study & Subjects
Hearing
Cochlea
Tinnitus
Genetics
Hearing Loss and Rehabilitation
Hearing Impairment and Communication
Publication details
- Journal / source
- Zenodo (CERN European Organization for Nuclear Research)
- Publication date
- 18 January 2026