慢性鼻-鼻窦炎
感音神经性聋
医学
发病机制
表型
免疫学
临床表型
听力损失
叙述性评论
听力学
免疫系统
感音神经性耳聋
重症监护医学
生物
基因
遗传学
作者
Aleksandar Perić,D Djerić
标识
DOI:10.1080/08820139.2024.2437638
摘要
Previous studies suggest that disrupted harmony between the immune response in the nasal and middle ear mucosa and inner ear structures may contribute to developing SNHL in CRS patients. This especially applies to CRS as part of NSAID-exacerbated respiratory disease and systemic necrotizing vasculitis, including GPA and EGPA. However, the exact mechanisms of development of SNHL in different forms of CRS have not been sufficiently investigated and new studies are necessary soon. Apart from the pathophysiological basis of SNHL, different therapeutic approaches in the clinical phenotypes of CRS have also been discussed.
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