Hearing Loss Secondary to <i>TECTA</i> Gene Mutations
<i>TECTA</i> gene variants are relatively common in this population, with c.3107G>A being the most frequent. The typical phenotype is slowly progressive, mid-to-high frequency sensorineural hearing loss, often starting in childhood and usually requiring hearing aids fitting with good results in improving speech intelligibility.
Authors
- Esther Onecha (ORCID: https://orcid.org/0000-0002-8631-3555)
- Carmelo Morales‐Angulo (ORCID: https://orcid.org/0000-0002-4268-2762)
- Rocío González‐Aguado (ORCID: https://orcid.org/0000-0002-4407-287X)
- Jaime Gallo‐Terán
Institutions
- Universidad de Cantabria (ES)
- Marqués de Valdecilla University Hospital (ES)
- Instituto de Investigación Marqués de Valdecilla (ES)
Publication Details
- Journal
- Annals of Otology Rhinology & Laryngology
- Published
- 2025-02-04
- DOI
- https://doi.org/10.1177/00034894251315550
- Primary Topic
- Hearing, Cochlea, Tinnitus, Genetics
- Type
- article
- Field-Weighted Citation Impact
- 0.00