Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

[Vogt-Koyanagi-Harada disease].

Ole Kjeka1, Jørgen Krohn

  • 1Øyeavdelingen, Haukeland Universitetssjukehus, 5021 Bergen. ole.kjeka@helse-bergen.no

Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|September 3, 2005
PubMed
Summary

Vogt-Koyanagi-Harada disease, a rare cause of bilateral uveitis, presents with vision loss and retinal detachment. Prompt high-dose corticosteroid treatment effectively resolves symptoms and improves vision.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

International validation of a staging system for ciliary body and choroidal melanomas using estimated tumour volume.

Canadian journal of ophthalmology. Journal canadien d'ophtalmologie·2026
Same author

A Randomized Trial of Tenecteplase in Acute Central Retinal Artery Occlusion.

The New England journal of medicine·2026
Same author

Fundus hypopigmentation and choroidal thinning associated with tebentafusp therapy: report of a case and literature review.

BMC ophthalmology·2025
Same author

Tenecteplase in Central Retinal Artery Occlusion Study (TenCRAOS): Protocol for a randomized-controlled trial.

European stroke journal·2025
Same author

Increasing Incidence of Posterior Uveal Melanoma in Scandinavia 1960-2022: A Tri-National Study.

American journal of ophthalmology·2025
Same author

Upright positioning facilitates the absorption of macular hole-related oedema.

Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie·2025

Area of Science:

  • Ophthalmology
  • Immunology

Background:

  • Vogt-Koyanagi-Harada disease is a rare autoimmune condition causing bilateral panuveitis.
  • It predominantly affects young adults, particularly those of Asian descent.
  • Commonly associated symptoms include meningeal signs, hearing loss, and pigmentary changes.

Observation:

  • Three patients with Vogt-Koyanagi-Harada disease presented with decreased vision.
  • Two patients experienced prodromal symptoms like headache and meningism.
  • All patients exhibited bilateral panuveitis with exudative retinal detachment and choroidal effusion.

Findings:

  • Fluorescein angiography revealed pinpoint hyperfluorescence and dye pooling.
  • High-dose systemic corticosteroids led to resolution of exudative retinal detachments.
  • All patients demonstrated improved visual acuity following treatment.

Implications:

  • Vogt-Koyanagi-Harada disease requires prompt diagnosis and management.
  • Early intervention with high-dose systemic steroids is crucial for favorable outcomes.
  • This condition is an important consideration in cases of bilateral uveitis.

Related Experiment Videos