Results 11 to 20 of about 4,988,152 (170)
Is it Vogt-Koyanagi-Harada syndrome?
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
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]
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
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]
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
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
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
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
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
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

