Correlation between the etiology of severe hearing loss and endolymphatic hydrops
Patients with genetic variants of GJB2, SLC26A4, LMX1A, younger patients, those with longer deaf durations showed a higher prevalence of vestibular and cochlear EH, implying EH appears to be formed as a developmental disorder in association with a certain set of genetic variants, rather than a phenotypic marker as a result of severe to profound hearing loss.
Authors
- Jin Hee Han
- J. Lee (ORCID: https://orcid.org/0000-0001-8462-9081)
- Sung-Min Park
- Byung Se Choi (ORCID: https://orcid.org/0000-0001-6310-1798)
- Byung Yoon Choi (ORCID: https://orcid.org/0000-0001-5125-2118)
- Yun Jung Bae (ORCID: https://orcid.org/0000-0002-1779-4949)
Institutions
- Seoul National University (KR)
- Seoul National University Bundang Hospital (KR)
- Hallym University Kangnam Sacred Heart Hospital (KR)
Publication Details
- Journal
- European Archives of Oto-Rhino-Laryngology
- Published
- 2024-10-07
- DOI
- https://doi.org/10.1007/s00405-024-08993-3
- Citations
- 1
- Primary Topic
- Vestibular and auditory disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.25
Funders
- Seoul National University Bundang Hospital
- Ministry of Trade, Industry and Energy
- Seoul National University Hospital