Abstract We aim to present multimodal imaging and treatment outcomes of a rare unilateral presentation of Vogt–Koyanagi–Harada (VKH) disease with a 1-year follow-up. A 49-year-old male reported with the unilateral blurring of vision for 1 month. On examination, features consistent with VKH disease were noted. Optical coherence tomography and fundus fluorescein angiography findings were typical of ocular involvement in VKH. The disease responded to steroids with complete resolution till the first relapse. The patient was started on azathioprine and showed marked improvement in visual acuity and disease activity.
Kumar et al. (Sun,) studied this question.