Cogan's syndrome is an inflammatory disease that is characterized by ocular
inflammation (typically interstitial keratitis) and is associated with Men
iere-like vestibuloauditory dysfunction, Ocular inflammation usually resolv
es after several weeks or months but deafness is often irreversible.
We report on a case of Cogan's syndrome in a 23-year-old woman who initiall
y presented with bilateral anterior uveitis, an unusual clinical feature fo
r this disease. We discuss the clinical aspects, the pathogenic mechanisms,
the laboratory investigations, the differential diagnosis, and the treatme
nt of Cogan's syndrome.