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, 2022 Vogt-Koyanagi-Harada (VKH) syndrome is a rare disorder that affects several body systems. Here we take a broad look at the presentation and pathophysiology of VKH, with a more specific focus on the relevant eye findings. Since much is not known about VKH,
Shwetha Mudalegundi, Medical Student; Amanda D. Henderson, MD
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Bilateral betrayal: When imaging calls out Vogt–Koyanagi–Harada’s one-eyed act
Indian Journal of Ophthalmology. Case ReportsWe report a case of asymmetric Vogt-Koyanagi-Harada syndrome mimicking unilateral Central Serous Chorioretinopathy. This case highlights the diagnostic challenge for making a correct diagnosis between asymmetric Vogt-Koyanagi-Harada disease and Central ...
Shagun Korla +2 more
doaj +1 more source
, 2018 Objective: To evaluate in which phase of Vogt-Koyanagi-Harada (VKH) syndrome the patients receive the first attendance in specialized service. Methods: A retrospective study was conduted to evaluate medical records of 14 patients with VKH in the ...
Giovanna Provenzano (5313341) +4 more
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Relato de Caso: Síndrome de Vogt-Koyanagi-Harada / Case Report: Vogt-Koyanagi-Harada Syndrome [PDF]
, 2021 Vogt–Koyanagi–Harada (VKH) disease is an inflammatory and autoimmune condition characterized by panuveitis, serous retinal detachments, and extraocular manifestations of the auditory, integumentary, and central nervous systems (CNS).
Caiado, Gustavo Coelho +3 more
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Cataract Surgery in Vogt — Koyanagi — Harada Syndrome (Clinical Case)
OftalʹmologiâThe article describes a clinical case of the Vogt — Koyanagi — Harada syndrome with an ophthalmic manifestations: bilateral granulomatous panuveitis with funnel-shaped serous retinal detachment complicated by cataracts, clinical manifestations in the ...
I. Yu. Razumova +4 more
doaj +1 more source
Aplicabilidade do critério diagnóstico revisado de 2001 em pacientes brasileiros com doença de Vogt-Koyanagi-Harada [PDF]
, 2008 PURPOSE: To determine the applicability of the international revised diagnostic criteria for Vogt-Koyanagi-Harada disease. METHODS: Retrospective study.
Zajdenweber, Moysés Eduardo [UNIFESP] +9 more
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Vogt-Koyanagi-Harada syndrome: A case report [Vogt-Koyanagi-Harada sendromu: Bir olgu sunumu]
, 2008 Vogt-Koyanagi-Harada syndrome is a rare, inflammatory disease with manifestations affecting the ocular, central nervous, auditory-vestibular systems. It affects pigmented individuals between 20-50 years old.
Koç F., Bozdemir H.
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Journal of Nepal Health Research CouncilBackground: To evaluate clinical characteristics and visual outcome of Vogt-Koyanagi-Harada disease patients in Nepal. Methods: Retrospective series of all the cases of VKH treated at Tilganga Institute of Ophthalmology from 1st July 2017 to 31st ...
Jyoti Bastola Paudel +2 more
doaj +1 more source
, 2017 peer reviewedWe present the case of a patient who had a decrease of the visual acuity associated with headaches, diagnosed as Vogt-Koyanagi-Harada syndrome. This is a rare multisystemic pathology that affects organs with high concentration of melanocytes.
DUCHATEAU, Edouard +2 more
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Vogt-koyanagi-harada syndrome [PDF]
, 2014 Vogt-Koyanagi-Harada (VKH) syndrome is a rare multisystem disease of melanocyte containing organs. It is characterized by diffuse granulomatous inflammation involving various organs including eye. VKH syndrome is usually sporadic, but some familial cases
Akram, Sharmeen, Ahmad, Khabir
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