Vogt-Koyanagi-Harada syndrome

Abstract

Vogt-Koyanagi-Harada Syndrome (VKH) is a rare condition accounting for less than 4% of uveitis referrals in the United States. This article reviews the ocular, neurologic, and integumentary manifestations of VKH. Treatment options for these patients are also presented. Given the low incidence of VKH, differential diagnosis for patients with panuveitis is also discussed.