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.

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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
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article

Hearing Loss Secondary to TECTA Gene Mutations

Esther Onecha, Carmelo Morales‐Angulo, Rocío González‐Aguado, Jaime Gallo‐Terán
Annals of Otology Rhinology & Laryngology
Hearing, Cochlea, Tinnitus, Genetics
article

Hearing Loss Secondary to TECTA Gene Mutations

Esther Onecha, Carmelo Morales‐Angulo, Rocío González‐Aguado, Jaime Gallo‐Terán
article en

Abstract

<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.

Annals of Otology Rhinology & LaryngologyVol. 134(6)
Universidad de Cantabria (ES), Marqués de Valdecilla University Hospital (ES), Instituto de Investigación Marqués de Valdecilla (ES)
Openalex Percentile: Top 98%
Hearing, Cochlea, Tinnitus, Genetics
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Hearing Loss Secondary to <i>TECTA</i> Gene Mutations — Esther Onecha, Carmelo Morales‐Angulo, et al. · Annals of Otology Rhinology & Laryngology (2025) | TGRS Research Map | TGRS