Concept information
Preferred term
Uveomeningoencephalitic Syndrome
Type
-
Topical Descriptor
Broader concept
Entry terms
- Disease, Vogt-Koyanagi-Harada
- Syndrome, VKH
- Syndrome, VKH (Vogt Koyanagi Harada)
- Syndrome, Vogt Koyanagi Harada
- Syndrome, Vogt-Koyanagi-Harada
- Uveomeningoencephalitides
- Uveomeningoencephalitis
- VKH Syndrome
- VKH Syndrome (Vogt Koyanagi Harada)
- VKH (Vogt Koyanagi Harada) Syndrome
- Vogt Koyanagi Harada Disease
- Vogt-Koyanagi-Harada Disease
- Vogt Koyanagi Harada Syndrome
- Vogt-Koyanagi-Harada Syndrome
Scope note
- 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)
History note
- 1991(1965); was see under UVEITIS 1965-1990
In other languages
-
Finnish
-
uveomeningoenkefaliittisyndrooma
-
Swedish
-
Uveomeningoencefalit
-
Vogt-Koyanagi-Haradas syndrom
URI
http://www.yso.fi/onto/mesh/D014607
{{label}}
{{#each values }} {{! loop through ConceptPropertyValue objects }}
{{#if prefLabel }}
{{/if}}
{{/each}}
{{#if notation }}{{ notation }} {{/if}}{{ prefLabel }}
{{#ifDifferentLabelLang lang }} ({{ lang }}){{/ifDifferentLabelLang}}
{{#if vocabName }}
{{ vocabName }}
{{/if}}