Analysis of deafness gene screening results in 15771 newborn cases in Anyang city of Henan
Implementing newborn genetic screening for deafness in this region facilitates the early identification of individuals at risk for congenital, delayed-onset, and aminoglycoside-induced hearing loss, enabling timely intervention and follow-up.
Authors
- Xue Li (ORCID: https://orcid.org/0009-0002-0863-5302)
- Zhonghua Li (ORCID: https://orcid.org/0000-0001-9380-2130)
- Haiyan Li (ORCID: https://orcid.org/0000-0001-8022-3447)
- Yanchao Mu
- Huiping An
- Yang Li (ORCID: https://orcid.org/0000-0002-7134-5685)
- Lei Zhang (ORCID: https://orcid.org/0000-0001-7242-5292)
- Dawei Wang (ORCID: https://orcid.org/0000-0002-4488-2135)
- MeiQing Han (ORCID: https://orcid.org/0009-0006-3757-9599)
- Di Hua (ORCID: https://orcid.org/0009-0005-6453-1016)
Institutions
- Fuyang Maternity and Child Health Care Hospital (CN)
- Liuyang City Maternal and Child Health Hospital (CN)
- Anyang Tumor Hospital (CN)
Publication Details
- Journal
- Frontiers in Pediatrics
- Published
- 2025-10-16
- DOI
- https://doi.org/10.3389/fped.2025.1645070
- Primary Topic
- Hearing, Cochlea, Tinnitus, Genetics
- Type
- article
- Field-Weighted Citation Impact
- 0.00