Results 21 to 30 of about 137,274 (148)

Unusual Case of Vogt-Koyanagi-Harada Syndrome Presenting as Non-specific Headache [PDF]

Journal of Clinical and Diagnostic Research, 2014
Vogt–Koyanagi–Harada syndrome (VKH) is a bilateral intraocular granulomatous panuveitis which is frequently associated with systemic manifestations such as meningismus, tinnitus, poliosis and vitiligoof autoimmune aetiology. Headache by itself, does not
Pradeep A.V., Arun Kumar J.S., Naveen K.N., Sonali Rao, Sharan Shetty   +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], Fimamor, Luciana Peixoto [UNIFESP], Rubens Belfort Jr., Muccioli, Cristina [UNIFESP], Luciana Peixoto Fimamor, Moysés Eduardo Zajdenweber, Cardoso, Isabel Habeyche [UNIFESP], Belfort, Rubens Junior [UNIFESP], Cristina Muccioli, Isabel Habeyche Cardoso   +9 more
core   +2 more sources

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

European 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, Sara Pérez Moyano, Husein Husein-ElAhmed, Ana María Alfaro Juárez   +3 more
doaj   +1 more source

Uveo-Meningeal Syndromes: Vogt-Koyanagi-Harada (VKH) Disease

, 2023
Ocular inflammatory symptoms with concurrent neuro-ophthalmologic manifestations can be diagnostically challenging. We provide a general overview of uveo-meningeal syndromes, which comprises a heterogeneous group of disorders that involve inflammation of
Rachana Haliyur, MD, PhD; Emily Cole, MD, MPH; Therese Sassalos, MD; Sangeeta Khanna, MD
core  

Macular Abnormalities in Vogt-Koyanagi-Harada Disease

, 2019
Purpose: To investigate the prevalence of macular abnormalities in Chinese Vogt-Koyanagi-Harada (VKH) patients. Methods: Clinical characteristics, therapeutic effectiveness and visual outcome were reviewed and analyzed.
Qingyun Zhou (391545), Aize Kijlstra (52532), Liping Du (301240), Jian Qi (345934), Zi Ye (302115), Jing Xu (15337), Liang Liang (19309), Chaokui Wang (351525), Chunjiang Zhou (5595575), Qingfeng Cao (561890), Lili Wu (559545), Peizeng Yang (42067)   +11 more
core   +2 more sources

Vogt-Koyanagi-Harada Syndrome in Two Patients with Immunoglobulin A Nephropathy [PDF]

, 2007
We describe herein 2 patients who developed Vogt-Koyanagi-Harada syndrome in the course of renal biopsy-proven immunoglobulin A (IgA) nephropathy. A 61-year-old man with an 11-year history of IgA nephropathy and a 16-year history of thyroiditis, and a 56-
Ota, Kosuke, Masuda, Ikuya, Nose, Soichiro, Sunami, Reiko, Yamadori, Ichiro, Matsuo, Toshihiko   +5 more
core   +1 more source

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

Dermatologica 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, Wooi Chiang Tan, Norazirah Md Nor   +2 more
doaj   +1 more source

Sindrome de Vogt-Koyanagi-Harada: relato de dois casos

Arquivos de Neuro-Psiquiatria, 1981
Os autores relatam a síndrome de Vogt-Koyanagi-Harada em duas mulheres adultas e de cor parda. São discutidos os aspectos clínicos, epidemiológicos, heredofamiliares e imunológicos.
Paulo E. Marchiori, Milberto Scaff, Dagoberto Callegaro, Noboru Yassuda, José Lamartine De Assis   +4 more
doaj   +1 more source

A Rare De Novo Missense Mutation in IFT122 Confers a Genetic Susceptibility Factor of Idiopathic Pediatric Uveitis Via Trio‐based Whole‐Exome Sequencing

Advanced Science, EarlyView.
A rare de novo IFT122‐A773E variant is identified in idiopathic pediatric uveitis and shown to exacerbate retinal inflammation and barrier dysfunction. Mechanistically, the variant enhances IFT43 interaction, elevates calcium signaling, and activates the MEK/ERK/FRA1 axis, revealing a previously unrecognized cilia‐associated pathway that may increase ...
Qian Zhou, Jiaxing Huang, Yilin Wang, Xingran Li, Xianyang Liu, Lingyu Dai, Hongshun Li, Qingfeng Wang, Jiangyi Liu, Guannan Su, Wanyun Zhang, Yang Deng, Qingfeng Cao, Yujie Lai, Xiang Luo, Changwei Huang, Ling Chen, Shengping Hou, Peizeng Yang   +18 more
wiley   +1 more source

A fingerprint hidden inside the eye. A unique pattern of outer retina splitting as seen on en-face OCT and OCT-angiography

American Journal of Ophthalmology Case Reports, 2021
A splitting of the outer plexiform retinal layer in a saw-like hyporeflective pattern in addition to partially formed concentric circles centred at the foveola were observed using en-face OCT and OCT-angiography in a 27-year-old female patient with ...
Tryfon Rotsos, Chrysanthos Symeonidis, Menelaos Kanakis, Konstantinos Andreanos   +3 more
doaj   +1 more source