Results 91 to 100 of about 137,343 (204)

Vogt koyanagi harada hastalığı

, 2011
On sekiz yaşında bayan hasta, şiddetli baş ağrısını takiben her iki gözünde görme kaybı ile başvurdu. Muayenesinde bilateral seröz retina dekolmanı, fundus fluoresein anjiografisinde multifokal noktasal sızıntı ve subretinal göllenme, ultrasonografisinde
Yaylalı, Volkan, Yaldızkaya, Filiz, Çetin, Ebru Nevin, Yıldırım, Cem   +3 more
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Sindrom Vogt-Koyanagi Harada Laporan Kasus

, 1998
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,
Perpustakaan UGM, i-lib
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Supplementary Material for: Atypical central serous chorioretinopathy masquerading as Vogt-Koyanagi-Harada disease: a case report.

Introduction: We aimed to describe a clinical presentation of central serous retinopathy that poses a diagnostic and management dilemma. Case presentation: A 30-year-old male patient presented with bilateral vision loss and multifocal serous retinal ...
Choi P. (18016015), Shieh D. (18429273), Ufret-Vincenty R.L. (18429279), Duran M. (4275412), He Y.-G. (18429276)   +4 more
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VOGT, KOYANAGI, HARADA (VKH) SYNDROME

Journal of Nepal Medical Association, 2003
D N Shah, PCD Karmacharya, S Koirala, M P Upadhayay   +3 more
doaj   +1 more source

Brain abscess caused by nocardia farcinica in a patient with Vogt-Koyanagi-Harada syndrome

Egyptian Journal of Neurosurgery
Background Nocardia brain abscess is extremely rare. Vogt-Koyanagi-Harada disease is an autoimmune driven inflammation of ocular, auditory and meningeal structures that all contain melanocyes, treated by high dose systemic steroid drugs and ...
Ravishankar S. Goel, Vikram Dua, Sachin Gupta, Reemu Bansal, Neha Rathor   +4 more
doaj   +1 more source

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  

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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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
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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
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