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Cogan syndrome (CS) is an autoimmune disease characterized by inflammation of the inner ears and the eyes, presenting with vestibulo-auditory dysfunction and interstitial keratitis. [1] The disease progresses over 3 to 90 days and usually shows a response to steroid treatment. [2]
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Cogan's syndrome is a rare entity, mostly described in young adult Caucasian patients of either sex, and fewer than 250 cases have been reported in the literature. Interstitial keratitis is rarely asymptomatic, and most of the patients present with eye redness, photophobia or eye pain [2, 3]. On examination of patients with IK, an irregular.
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Cogan syndrome is a rare autoimmune disease involving the eye and the inner ear. Cogan syndrome affects young adults, with 80% of patients between 14 and 47 years. The disease appears to result from an autoimmune reaction directed against an unknown common autoantigen in the cornea and inner ear. About 10 to 30% of patients also have severe.
