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Uveomeningoencephalitic Syndrome

More information in Books or onNLM PubMed
Definition: A syndrome characterized by bilateral granulomatous UVEITIS with IRITIS and secondary GLAUCOMA, premature ALOPECIA, symmetrical VITILIGO, poliosis circumscripta (a strand of depigmented hair), HEARING DISORDERS, and meningeal signs (neck stiffness and headache). Examination of the cerebrospinal fluid reveals a pattern consistent with MENINGITIS, ASEPTIC. (Adams et al., Principles of Neurology, 6th ed, p748; Surv Ophthalmol 1995 Jan;39(4):265-292)  DF: UVEOMENINGOENCEPH SYNDROME    Other names Vogt-Koyanagi-Harada Syndrome; Uveomeningoencephalitis; Vogt Koyanagi Harada Syndrome; Vogt Koyanagi Harada Disease; VKH Syndrome (Vogt Koyanagi Harada); Uveomeningoencephalitides; Syndrome, Vogt-Koyanagi-Harada; Syndrome, VKH; Syndrome, Uveomeningoencephalitic; Disease, Vogt-Koyanagi-Harada; Vogt-Koyanagi-Harada Disease; VKH Syndrome; VKH (Vogt Koyanagi Harada) Syndrome; Syndrome, Vogt Koyanagi Harada; Syndrome, VKH (Vogt Koyanagi Harada)

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Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012

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