Vogt-Koyanagi-Harada syndrome is a rare autoimmune multiorgan disease that is characterized by granulomatous uveitis with a spectrum of auditory, neurological and skin manifestations.
Bilateral involvement, occurring either at the time of presentation or sequentially, is considered a hallmark of Vogt-Koyanagi-Harada (VKH) disease and is proposed as a diagnostic criterion by the International Workshop on Vogt-Koyanagi-Harada Disease, yet case reports of unilateral VKH disease exist in the literature. In this column, we report an atypical case of VKH in a one-eyed patient whose clinical course
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