A5006869842- Hearing, Cochlea, Tinnitus, Genetics
- Vestibular and auditory disorders
- Hearing Loss and Rehabilitation
- Ear Surgery and Otitis Media
- Noise Effects and Management
- Multisensory perception and integration
- Pediatric health and respiratory diseases
- Nasal Surgery and Airway Studies
- Voice and Speech Disorders
- Ion channel regulation and function
- Speech and Audio Processing
- Glaucoma and retinal disorders
Guizhou Provincial People's Hospital
2018-2024
Pioneer (United States)
2023
Cardiff Metropolitan University
2019
Government of Jiangsu Province
1991
Deafness autosomal dominant 2A (DFNA2A) is related to non-syndromic genetic hearing impairment. The KCNQ4 (Potassium Voltage-Gated Channel Subfamily Q Member 4) can lead DFNA2A. In this study, we report a case of loss with six family members as caused by novel variant in the gene.
Objective:To investigate the difference of therapeutic effect tinnitus patients with different types hearing curve.Method:Patients inclusion and exclusion criteria for treatment were studied retrospectively.Use SPSS 20.0 Chinese version software to collect data analysis.The was statistically significant when P<0.05.Result:A total 164 collected, most curve high frequency loss; according TEQ scoring grading method, in middle severity; The chi-square test showed that there no among first...