Results 91 to 100 of about 137,274 (148)

Clinical course of focal choroidal excavation in Vogt–Koyanagi–Harada disease

Clinical Ophthalmology, 2014
Yuko Nishikawa,1–3,* Kaoru Fujinami,1,2,4,5,* Ken Watanabe,1,2 Toru Noda,1,2 Kazushige Tsunoda,1,2 Kunihiko Akiyama1,2 1Department of Ophthalmology, National Hospital Organization, Tokyo Medical Center, Tokyo, Japan; 2Laboratory of Visual ...
Nishikawa Y, Fujinami K, Watanabe K, Noda T, Tsunoda K, Akiyama K   +5 more
doaj  

An Unusual Presentation of Vogt–Koyanagi–Harada

Journal of Ophthalmic & Vision Research, 2021
Sefik Can Ipek, Sadettin Uslu, Gercek Can, Ozlem Ozbagcivan, Pinar Cakar Ozdal, Ali Osman Saatci   +5 more
doaj   +1 more source

不典型Vogt-小柳原田综合征误诊1例

Zhongguo shiyan zhenduanxue, 2012
Vogt-小柳原田综合征（Vogt-Koyanagi-Harada syndrome,VKH综合征）是一种目前病因尚不明确,以双侧肉芽肿性全葡萄膜炎为特征的疾病[1]。该病因早期表现多样,缺乏特异性诊断标准,在我国误诊、漏诊率极高。本文报道临床误诊为原发性闭角型青光眼的VKH综合征1例,分析原因以引起重视。
赵婧, 郑雅娟, 郝继龙
doaj  

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

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  

Sindroma Vogt-Koyanagi-Harada: apresentação clinica atipica?

, 2013
INTRODUÇÃO Síndroma de Vogt-Koyanagi-Harada (SVKH) é uma doença inflamatória rara, de etiologia desconhecida e multissistémica, caracterizada por uma panuveite bilateral associada a manifestações dermatológicas, auditivas e meníngeas.
Ramalho, M, Teixeira, S, Santos, C, Bernardo, M, Coutinho, I, Pedrosa, C, Amaral, N   +6 more
core  

Vogt-Koyanagi-Harada Syndrome: A case report

, 2015
The Vogt-Koyanagl-Harada Syndrome is characterized by bilateral panuveitis and exudative retinal detachments, in association with cutaneous and neurosensory manifestations. This syndrome is seen most commonly in darker pigmented races, such as Orientals,
Suhardjo, Suhardjo
core   +1 more source

Delayed cutaneous depigmentation in Vogt-Koyanagi-Harada disease. [PDF]

Skin Health Dis
Shanshal M, Khan S.
europepmc   +1 more source

Progressive Subretinal Fibrosis Complicating Vogt-Koyanagi-Harada Syndrome during Systemic Corticosteroid Treatment

, 2009
We describe 2 patients with Vogt-Koyanagi-Harada syndrome in whom the development of markedly progressive subretinal fibrosis and telangiectasis over the optic disc showed peculiar manifestations.
CHEN, MUH-SHY, 陳慕師
core  

Enfermedad de Vogt-Koyanagi-Harada y rehabilitación visual

Revista Cubana de Oftalmología
La enfermedad de Vogt-Koyanagi-Harada es una entidad infrecuente, multisistémica, de etiología desconocida, presuntamente autoinmune, caracterizada por panuveítis granulomatosa crónica bilateral y difusa, acompañada de participación tegumentaria ...
Mayrelis Quintero Busutil, Daysi Caridad Vilches Lescalle, Yurania Bueno Arrieta, Susana Rodríguez Masó, Carlos Alberto Perea Ruíz, Miladis Paz Lorenzo   +5 more
doaj  

Vogt-Koyanagi-Harada Disease Presenting With Progressive Visual Loss and Multisystem Involvement: A Case Report. [PDF]

Am J Case Rep
Elshweikh SA, Almutairi AG, Thalib HI, Alolayan RW, Aly MM.   +4 more
europepmc   +1 more source