Results 81 to 90 of about 1,359,849 (169)
Enfermedad de Vogt Koyanagi Harada Bilateral: Reporte de un Caso [PDF]
Objetivo: Reportar el caso de una paciente diagnosticada con Enfermedad de Vogt Koyanagi Harada bilateral. Caso Clínico: Paciente femenina de 42 años, sin antecedentes médicos de importancia, quien consulta por visión borrosa en ojo derecho de 2 ...
Flor de María Chew Florián
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Intravascular lymphoma masquerading as Vogt-Koyanagi-Harada syndrome
PURPOSE: To describe the clinical course of a case of intravascular lymphoma. DESIGN: Case report. METHODS: Retrospective chart review. RESULTS: A 56-year-old man presented with blurry vision associated with fever and decreased hearing.
Zabar, Yuval +8 more
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Presumed atypical peripapillary Vogt-Koyanagi-Harada disease
Purpose: To describe a case of bilateral presumed atypical Harada disease with sequential, not simultaneous, involvement of the peripapillary retina (subretinal fluid) in a healthy patient with no systemic complaints.
Julio Zaki Abucham-Neto +4 more
doaj +1 more source
Vogt-Koyanagi-Harada syndrome - current perspectives [PDF]
Vogt-Koyanagi-Harada syndrome is a cause of noninfectious panuveitis, leading to significant vision loss in many patients. It is an autoimmune disease occurring in genetically susceptible individuals and clinically presents as bilateral panuveitis with ...
Tomkins-Netzer, O +2 more
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Bilateral disc edema in a patient with Vogt-Koyanagi-Harada disease
OAIID:oai:osos.snu.ac.kr:snu2014-01/102/0000004487/16SEQ:16PERF_CD:SNU2014-01EVAL_ITEM_CD:102USER_ID:0000004487ADJUST_YN:YEMP_ID:A075641DEPT_CD:801CITE_RATE:1.299FILENAME:yang hk-vogt koyanagi-harada-can j ophthalmol-2014-49(2)e54.pdfDEPT_NM:의학과SCOPUS_YN:
Yang, Hee Kyung +4 more
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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: A Case Report
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Filiz Koç, Hacer Bozdemir
doaj
Vogt-koyanagi-harada syndrome [PDF]
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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Clinical features of the investigated BD and VKH syndrome patients.
BD, Behcet's disease; VKH, Vogt–Koyanagi–Harada syndrome.
Qingyun Zhou (391545) +7 more
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Brain abscess caused by nocardia farcinica in a patient with Vogt-Koyanagi-Harada syndrome
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 +4 more
doaj +1 more source

