Uveomeningoencephalitic Syndrome
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)
Year introduced: 1991(1965)
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Subheadings:
Tree Number(s): C10.114.843, C11.941.879.980, C20.111.258.925
MeSH Unique ID: D014607
Entry Terms:
- Syndrome, Uveomeningoencephalitic
- Vogt-Koyanagi-Harada Syndrome
- Syndrome, Vogt-Koyanagi-Harada
- Vogt Koyanagi Harada Syndrome
- Uveomeningoencephalitis
- Uveomeningoencephalitides
- Syndrome, Vogt Koyanagi Harada
- Syndrome, VKH (Vogt Koyanagi Harada)
- VKH Syndrome (Vogt Koyanagi Harada)
- Vogt-Koyanagi-Harada Disease
- Disease, Vogt-Koyanagi-Harada
- Vogt Koyanagi Harada Disease
- VKH (Vogt Koyanagi Harada) Syndrome
- VKH Syndrome
- Syndrome, VKH