DR. UJJWALA PANDEY

DR.JYOTI BHUYAN, DR.RITA DEKA

Abstract

Vogt–Koyanagi–Harada (VKH) syndrome is a multisystemic autoimmune disease. It is a non-necrotizing diffuse granulomatous uveitis disease, commonly affecting various organs such as eyes, central nervous system, inner ear, and skin.[12] It is characterized by ocular signs such as panuveitis, serous or exudative retinal detachment, “sunset glow fundus” with optic disk hyperemia, neurologic signs like tinnitus, headache, meningitis, and cranial nerve palsies, and dermatologic signs like alopecia, vitiligo, and poliosis. A 32 year old female presented to the ophthalmology outpatient department with blurring of vision since 5 months with vitiligo patches over her face