Hearing loss trajectory and prediction model for children with enlarged vestibular aqueduct
These findings reveal that the PTT would deteriorate over time in patients with EVA. The hearing threshold at high frequency and genotype without c.919-2 A > G heterozygous mutation deteriorated relatively fast. Genotype is an important predictive factor and the nomogram helps to predict progressive hearing loss.
Authors
- Junfang Xian (ORCID: https://orcid.org/0000-0003-2191-9393)
- Yiding Yu (ORCID: https://orcid.org/0000-0002-2081-3709)
- Hui En
- Jinge Xie
- Wen Cheng (ORCID: https://orcid.org/0000-0003-3975-0389)
- Xiaozhe Yang (ORCID: https://orcid.org/0000-0002-0190-5114)
- Lihui Huang
- Dongxin Liu (ORCID: https://orcid.org/0000-0002-0956-5142)
- Xiaohua Cheng
- Shan Gao (ORCID: https://orcid.org/0009-0001-8124-9128)
- Hui Liu (ORCID: https://orcid.org/0000-0001-9531-9142)
- Yue Li (ORCID: https://orcid.org/0000-0002-7216-3488)
- Lin Deng (ORCID: https://orcid.org/0009-0000-0467-1766)
- Yu Ruan
Institutions
- Beijing Tongren Hospital (CN)
- Capital Medical University (CN)
Publication Details
- Journal
- American Journal of Otolaryngology
- Published
- 2024-12-20
- DOI
- https://doi.org/10.1016/j.amjoto.2024.104573
- Citations
- 2
- Primary Topic
- Hearing, Cochlea, Tinnitus, Genetics
- Type
- article
- Field-Weighted Citation Impact
- 0.72