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Cogan syndrome

MONDO:0015453

Cogan syndrome (CS) is a rare autoimmune disorder of unknown origin characterized by inflammatory ocular disease (mainly interstitial keratitis) and vestibulo-auditory manifestations (mainly acute onset hearing loss, tinnitus and vertigo), in the setting of a negative work-up for syphilis, with a variable risk of developing into a systemic disease. Systemic manifestations may occur in more than 70% of cases.

Also known as: Cogan syndrome

35 clinical trials for this condition and its sub-types, 0 tagged with Cogan syndrome itself.

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