Vogt-Koyanagi-Harada disease

A bilateral, chronic, diffuse granulomatous panuveitis typically characterized by serous retinal detachment and frequently associated with neurological (meningitis), auditory, and dermatological alterations.

Also known as: Harada's disease, Uveomenigitic syndrome, Vogt-Koyanagi syndrome, uveomeningoencephalitic syndrome, VKH disease, VKH syndrome, Vogt-Koyanagi-Harada syndrome

24 clinical trials for this condition and its sub-types.