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- W2800793223 abstract "Cogan’s syndrome (CS) is a rare autoimmune disorder characterized by audiovestibular dysfunction and ocular inflammation. Currently, there is no specific serum autoantibody used in the diagnostic workup of CS. Treatment is based on immunosuppressive agents, mainly corticosteroids as first-line choice. Recently, novel therapeutic modalities in CS have emerged. These include tumor necrosis factor- α inhibitors and other biologicals. Despite medical treatment, hearing loss may progress to irreversible bilateral profound SNHL in approximately half of CS patients resulting in candidacy for cochlear implantation (CI). Due to the inflammatory nature of the disease that is causing endosteal reaction with partial obliteration or complete neoossification of the intracochlear ducts, early CI is recommended. CI provides excellent and stable hearing rehabilitation with high score of word and sentence recognition. In this review, we will discuss different aspects of CS including clinical presentation, diagnosis, treatment, and future directives." @default.
- W2800793223 created "2018-05-17" @default.
- W2800793223 creator A5028592304 @default.
- W2800793223 creator A5058594488 @default.
- W2800793223 creator A5063591705 @default.
- W2800793223 date "2018-01-01" @default.
- W2800793223 modified "2023-10-03" @default.
- W2800793223 title "Autoimmune Inner Ear Disease: Immune Biomarkers, Audiovestibular Aspects, and Therapeutic Modalities of Cogan’s Syndrome" @default.
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- W2800793223 doi "https://doi.org/10.1155/2018/1498640" @default.
- W2800793223 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5937438" @default.
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- W2800793223 hasPublicationYear "2018" @default.
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