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[The Vogt-Koyanagi-Harada uveomeningoencephalitic syndrome].

Authors: H, Menger; W, Neukäter; S, Kroll; J, Jörg;

[The Vogt-Koyanagi-Harada uveomeningoencephalitic syndrome].

Abstract

VKHS is an inflammatory system disease with a subacute chronic course. It has a very variable, selective involvement of certain pigment cells of the eye, skin, inner ear, and meninges. Due in part to the fact that its symptoms are responsive to immunosuppressive therapy, pathogenesis as an autoimmune disease is considered. The clinical course of one of our patients is discussed. Early diagnosis of VKHS, although often very difficult, is mandatory for appropriate and timely treatment.

Keywords

Adult, Male, Dose-Response Relationship, Drug, Magnetic Resonance Imaging, Drug Administration Schedule, Autoimmune Diseases, Cortisone, Diagnosis, Differential, Leukocyte Count, Azathioprine, Humans, Fluorescein Angiography, Visual Fields, Uveomeningoencephalitic Syndrome

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Powered by OpenAIRE graph
Found an issue? Give us feedback
citations
The total number of citations received by all articles of the researcher of interest.
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
2
Average
Average
Average
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