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Vogt–Koyanagi–Harada Disease

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Abstract

Vogt–Koyanagi–Harada disease is a bilateral granulomatous panuveitis, generally symmetrical, associated to extraocular manifestations such as poliosis, vitiligo, alopecia, central nervous system, and auditory signs. It is considered an autoimmune disease, mediated by T cells, against melanocytes of uveal tract, skin, central nervous system, and inner ear. A genetic predisposition has been suggested. Patients have no history of ocular trauma and no clinical or laboratory evidence of other ocular or systemic disease. Therapy includes early, high doses of systemic steroids. Immunomodulatory therapy has also been used with good results.

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de Lourdes Arellanes-García, M., Concha-del-Río, L.E., del Carmen Preciado-Delgadillo, M., Recillas-Gipsert, C. (2013). Vogt–Koyanagi–Harada Disease. In: Arévalo, J. (eds) Retinal and Choroidal Manifestations of Selected Systemic Diseases. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-3646-1_19

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