Characteristics of Hearing Loss in Patients with COL2A1 Gene Variants (Sticker Syndrome Type 1)
María Fábrega-Torrano, Rocío González-Aguado, Esther Onecha, Carmelo Morales-Angulo

TL;DR
This study examines hearing loss in patients with Stickler syndrome type 1, finding that it is common and often sensorineural, requiring interventions like hearing aids or cochlear implants.
Contribution
The study provides new insights into the variability and management of hearing loss in patients with COL2A1 gene variants.
Findings
75% of patients with Stickler syndrome type 1 exhibited hearing loss ranging from mild to profound.
Sensorineural hearing loss was the most common type, requiring hearing aids or cochlear implants in some cases.
One patient required a mastoidectomy due to cholesteatoma associated with conductive hearing loss.
Abstract
Stickler syndrome type 1 (STL1) is an autosomal dominant genetic disorder that affects connective tissue with highly heterogeneous clinical manifestations, primarily at the ocular, orofacial, skeletal, and auditory levels. The aim of our study was to determine the variability of the auditory phenotype associated with pathogenic variants of the COL2A1 gene and its impact on long-term treatment and follow-up. A retrospective observational study was conducted on patients with a confirmed diagnosis of STL1 treated between 2018 and 2024 at the Otorhinolaryngology Department of the Marqués de Valdecilla University Hospital. The electronic medical records of the patients included in the study were reviewed to gather the following information: family history, age, sex, genetic variant of STL1, audiological test data, associated clinical manifestations, radiological tests, and treatment. Among…
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Taxonomy
TopicsConnective tissue disorders research · Tracheal and airway disorders · Congenital heart defects research
