Results 11 to 20 of about 2,875 (111)
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. +4 more
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Harada-like syndrome post-Covishield vaccination: A rare adverse effect
Indian Journal of Ophthalmology, 2022 Covishield is in wide use in India with about 80% efficacy. Serious side effects are still under study. A 30-year-old female presented to us 7 days post-vaccination with a 5-day history of sudden diminution of vision in both eyes.
Yogya Reddy +3 more
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Is it Vogt-Koyanagi-Harada syndrome?
Medical Journal of Dr. D.Y. Patil University, 2015 Vogt-Koyanagi-Harada syndrome (VKH syndrome) is named after ophthalmologists Alfred Vogt from Switzerland and Yoshizo Koyanagi and Einosuke Harada from Japan.
Digambar Dashatwar +2 more
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Vogt-Koyanagi-Harada syndrome: a discussion about resistance to corticotherapy
Revista Brasileira de Oftalmologia, 2021 Vogt-Koyanagi-Harada (VKH) syndrome is an inflammatory condition of unknown etiology that can affect the eye. The most common ocular manifestation related to VKH is bilateral diffuse uveitis associated to exudative retinal detachment.
Natália de Carvalho Dias +1 more
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Multimodal imaging in pediatric uveitis
Therapeutic Advances in Ophthalmology, 2021 Pediatric uveitis accounts for up to 10% of all uveitis cases, so special attention must be paid to ensure early diagnosis as well as treatment and follow-up of these young patients in order to decrease the risk of possible ocular complications and ...
Fitz Gerald I. Diala +3 more
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Journal of Translational Medicine, 2023 Background Uveitis and posterior scleritis are sight-threatening diseases with undefined pathogenesis and accurate diagnosis remains challenging. Methods Two plasma-derived extracellular vesicle (EV) subpopulations, small and large EVs, obtained from ...
Lingzi Wu +12 more
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Panuveite révélant une maladie de Vogt Koyanagi Harada (A propos de trois cas)
Journal de la Société Marocaine d’Ophtalmologie, 2015 Le syndrome de voght koyanagi harada (VKH) est une uvéo méningite bilatérale d’origine auto-immune, le diagnostic repose sur l’association variable de signes oculaires, méningés , auditifs et cutanés, le traitement repose sur les bolus de corticothérapie
G. El houari +9 more
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Asymmetric and incomplete vogt Koyanagi – Harada syndrome: Patient's perceptive dilemma
TNOA Journal of Ophthalmic Science and Research, 2022 Vogt–Koyanagi–Harada (VKH) is a rare autoimmune multisystem disease. Here, we report a case of VKH with asymmetric involvement and the importance of patient counselling and a comprehensive approach. A 45-year-old female patient went to tertiary care with
Priyanka H Gandhi +3 more
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TNOA Journal of Ophthalmic Science and Research, 2022 Inflammation of sclera with involvement of uvea is an uncommon and underdiagnosed disease entity seen in an ophthalmological outpatient setting. A 34-year-old male presented with complaints of headache, redness, pain, photophobia, and blurring of vision ...
Purva Vijay Deore +3 more
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Vogt-Koyanagi-Harada syndrome presenting with encephalopathy
Annals of Indian Academy of Neurology, 2014 Vogt-Koyanagi-Harada (VKH) is a rare syndrome affecting tissues containing melanocytes. The possibility of its autoimmune pathogenesis is supported by high frequent HLA-DR4 presentation, commonly associated with other autoimmune diseases.
Alireza E Naeini +3 more
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