Bilgic, OzlemGunduz, AbuzerKaya, Kismet2020-03-262020-03-2620140736-80461525-1470https://dx.doi.org/10.1111/pde.12163https://hdl.handle.net/20.500.12395/31279Vogt-Koyanagi-Harada (VKH) disease is a rare multiorgan disorder that affects the melanocytes of the eyes, skin, inner ear, and meninges. It is more common in women and in patients 30 to 50 years of age; it is rarely seen in children. We report a 14-year-old boy who meets the criteria for complete VKH disease.en10.1111/pde.12163info:eu-repo/semantics/closedAccessArticle3119910123869531Q2WOS:000330951800033Q3