Concept information
Preferred term
Uveomeningoencephalitic Syndrome
Type
-
mesh:Descriptor
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)
Broader concept
Entry terms
- Syndrome, VKH (Vogt Koyanagi Harada)
- Syndrome, Vogt Koyanagi Harada
- Uveomeningoencephalitis
- VKH Syndrome
- VKH (Vogt Koyanagi Harada) Syndrome
- Vogt-Koyanagi-Harada Disease
- Vogt-Koyanagi-Harada Syndrome
Allowable Qualifier(s)
- blood (Qualifier)
- cerebrospinal fluid (Qualifier)
- chemically induced (Qualifier)
- classification (Qualifier)
- complications (Qualifier)
- congenital (Qualifier)
- diagnosis (Qualifier)
- diagnostic imaging (Qualifier)
- diet therapy (Qualifier)
- drug therapy (Qualifier)
- economics (Qualifier)
- embryology (Qualifier)
- enzymology (Qualifier)
- epidemiology (Qualifier)
- ethnology (Qualifier)
- etiology (Qualifier)
- genetics (Qualifier)
- history (Qualifier)
- immunology (Qualifier)
- metabolism (Qualifier)
- microbiology (Qualifier)
- mortality (Qualifier)
- nursing (Qualifier)
- parasitology (Qualifier)
- pathology (Qualifier)
- physiopathology (Qualifier)
- prevention & control (Qualifier)
- psychology (Qualifier)
- radiotherapy (Qualifier)
- rehabilitation (Qualifier)
- surgery (Qualifier)
- therapy (Qualifier)
- urine (Qualifier)
- veterinary (Qualifier)
- virology (Qualifier)
In other languages
-
French
-
Maladie d'Harada
-
Maladie de Vogt-Koyanagi-Harada
-
Syndrome de Vogt-Koyanagi-Harada
-
Syndrome uvéoméningoencéphalique
-
Syndrome VKH
-
Uvéo-méningo-encéphalite
-
Uvéo-méningo-encéphalite d'Harada
-
Uvéoméningoencéphalite
URI
http://data.loterre.fr/ark:/67375/JVR-B1HRJ03V-8
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