Analysis of Serum Inflammatory Markers in Infants Under 6 Months of Age with Non-Syndromic Moderate and Severe Hearing Loss Associated with GJB2 Gene Mutations

BACKGROUND: The GJB2 gene is reported to be the main hereditary factor responsible for non-syndromic hearing impairment in infants. Several kinds of hearing loss have been linked to elevated inflammatory markers. This study aimed to evaluate serum levels of IL-2, IL-4, IL-6, IL-10, IL-17, α-TNF, and...

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Detalles Bibliográficos
Autores principales: Zhang, Xingang, Ma, Zhaoxin, Zheng, Jishan, Xu, Huiqing, Pan, Jiewen, Lv, Lanqiu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2023
Materias:
Clinical Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9825025/
https://www.ncbi.nlm.nih.gov/pubmed/36593740
http://dx.doi.org/10.12659/MSM.938165

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9825025/
https://www.ncbi.nlm.nih.gov/pubmed/36593740
http://dx.doi.org/10.12659/MSM.938165

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