Abstract
Vogt-Koyanagi-Harada disease (VKH) is a granulomatous inflammatory disorder affecting the eyes, auditory system, meninges, and skin. An association with ocular inflammation and poliosis was reported by Vogt in 1906. Harada (1926) and Koyanagi (1929) independently described ocular inflammation associated with cerebrospinal fluid pleocytosis and dermal depigmentation, respectively. Later, the disorders described by Vogt, Koyanagi, and Harada were considered to be the same disease process, which came to be known as VKH.
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The authors thank Dr. Izumi Yamamoto and Dr. Shigeaki Ohno for providing the illustrations.
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Vogt Koyanagi-Harada (PPT 5861 kb)
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Vogt-Koyanagi Harada disease (PPT 9980 kb)
Case Report 47
Atypical case of Vogt-Koyanagi-Harada (PPT 3338 kb)
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Kase, S., Rao, N.A. (2016). Vogt-Koyanagi-Harada Disease. In: Zierhut, M., Pavesio, C., Ohno, S., Orefice, F., Rao, N. (eds) Intraocular Inflammation. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-75387-2_96
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DOI: https://doi.org/10.1007/978-3-540-75387-2_96
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