Results 81 to 90 of about 137,274 (148)

Pattern of uveitis in North East India: A tertiary eye care center study

Indian Journal of Ophthalmology, 2009
We conducted an institutional-based retrospective study on 308 uveitic patients and analyzed the pattern of uveitis in Northeastern India. Anterior uveitis was the most common type (47.07%) followed by posterior (29.87%), intermediate (12 ...
Das Dipankar, Bhattacharjee Harsha, Bhattacharyya Pankaj, Jain Lokesh, Panicker M, Das Kalyan, Deka Akshay   +6 more
doaj  

Síndrome Uveomeningeo Vogt-Koyanagi-Harada

, 2017
El síndrome Vogt-Koyanagi-Harada es una panuveitis granulomatosa bilateral que cursa con desprendimiento de retina seroso y que puede acompañarse de afectación del sistema nervioso central, alteraciones dermatológicas y auditivas1.
Alejos Ramirez, Luis E., Garzarán Tejeiro, Ana, Pastor Espuig, M.   +2 more
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TUBERCULOUS CHOROIDITIS IN PATIENT WITH VOGT-KOYANAGI-HARADA DISEASE.

, 2018
To describe a novel case of intraocular tuberculosis (TB) arising in a patient undergoing treatment for Vogt-Koyanagi-Harada disease, and to highlight the use of spectral domain optical coherence tomography for helping confirm the diagnosis and monitor ...
Jonisch, J., El Khoury, L., Schwartzman-Morris, J. S., Anderson, E. W., Goldberg, N. R.   +4 more
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Evolución severa en Enfermedad de Vogt-Koyanagi-Harada

, 1986
We present the severe evolution of Vogt-Koyanagi-Harada disease with corticotherapy and immunosuppresive treatment.Presentamos la evolución severa de la enfermedad de Vogt-KoyanagiHarada a pesar del tratamiento corticoideo e inmunosupresor ...
Herrera Piñero, R., Castellano Solanes, Jorge, Gil Hernández, María A., Hernández Brito, Ana María, Abreu Reyes, Pedro   +4 more
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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

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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