Results 11 to 20 of about 4,988,152 (170)

Is it Vogt-Koyanagi-Harada syndrome?

open access: yesMedical Journal of Dr. D.Y. Patil University, 2015
Vogt-Koyanagi-Harada syndrome (VKH syndrome) is named after ophthalmologists Alfred Vogt from Switzerland and Yoshizo Koyanagi and Einosuke Harada from Japan.
Digambar Dashatwar   +2 more
doaj   +2 more sources

Echographic findings in the late stages of Vogt-Koyanagi-Harada disease in mexican population

open access: yesRevista Brasileira de Oftalmologia, 2014
Purpose: To correlate clinical findings of Vogt-Koyanagi-Harada disease with standardized echography findings in a cross-sectional, descriptive and observational study.
Mariana Mayorquín-Ruiz   +4 more
doaj   +2 more sources

Vogt-Koyanagi-Harada disease, a rare entity in Spain: the challenge of worldwide immigration and globalization [PDF]

open access: yesEuropean Journal of Case Reports in Internal Medicine, 2018
Vogt–Koyanagi–Harada disease is rare, mediated by autoimmune melanocyte inflammation and facilitated by genetic predisposition[1-3]. The main clinical features include uveitis, meningitis, tinnitus and sensorineural deafness, and skin and hair ...
Alberto Benavente Fernández   +3 more
doaj   +2 more sources

A Case of Probable Vogt-Koyanagi-Harada Disease

open access: yesTürk Oftalmoloji Dergisi, 2012
The aim of this article is to present a rare form of Vogt-Koyanagi-Harada (VKH) disease. The complete and incomplete forms of VKH disease are more frequent than the probable form.
Mutlu Acar   +3 more
doaj   +2 more sources

Vogt-Koyanagi-Harada disease. [PDF]

open access: yes, 2019
Vogt-Koyanagi-Harada disease is a rare, multisystem, autoimmune disorder with numerous clinical manifestations, mediated through a T-helper 1 response against melanocytes in the eye, inner ear, central nervous system, hair and skin. We describe a 20-year-
Mollan, Susan P   +3 more
core   +2 more sources

A case presentation of an IgA nephropathy patient with Vogt-Koyanagi-Harada syndrome

open access: yesBMC Nephrology, 2020
Background Vogt-Koyanagi-Harada syndrome is a rare disease characterized by skin and eyelash bleaching, chronic granulomatous iridocyclitis and exudative retinal detachment, and aseptic meningitis and encephalopathy.
Quan Zhang   +3 more
doaj   +1 more source

Chromatin accessibility analysis reveals regulatory dynamics and therapeutic relevance of Vogt-Koyanagi-Harada disease

open access: yesCommunications Biology, 2022
Single-cell RNA-sequencing and chromatin accessibility analysis reveal transcriptomic and epigenomic changes between healthy patients and those affected by the systemic autoimmune disorder Vogt-Koyanagi-Harada disease.
Wen Shi   +9 more
doaj   +1 more source

Hints from the skin beneath: Vitiligo in Vogt–Koyanagi–Harada disease

open access: yesDermatologica Sinica, 2022
Vogt–Koyanagi–Harada disease (VKHD) is a major vision-threatening autoimmune disease. One of its associated features is vitiligo. Little study has been done on the association between vitiligo and the disease activity of VKHD.
Jo Anne Lim   +2 more
doaj   +1 more source

Pigmented paravenous retinochoroidal atrophy associated with Vogt-Koyanagi-Harada disease: a case report

open access: yesBMC Ophthalmology, 2020
Background To describe a unique case of pigmented paravenous retinochoroidal atrophy that developed several years after Vogt-Koyanagi-Harada disease. Case presentation A 28-year-old woman presented with gradual vision loss in both eyes and nyctalopia for
Prithvi Ramtohul   +3 more
doaj   +1 more source

A COVID-19 perspective of Vogt–Koyanagi–Harada disease

open access: yesIndian Journal of Ophthalmology, 2023
Vogt–Koyanagi–Harada (VKH) disease, a bilateral granulomatous panuveitis associated with multisystem involvement, is a T-cell-mediated autoimmune disorder in which cytotoxic T-cell target melanocytes in genetically susceptible individuals.
Parthopratim Dutta Majumder   +3 more
doaj   +1 more source

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