Results 101 to 110 of about 4,991,692 (213)
Clinical spectrum and management options in Vogt–Koyanagi–Harada disease
, 2017 Sikander AK Lodhi, JM Lokabhi Reddy, Venkataratnam Peram Department of Ophthalmology, Osmania Medical College/Sarojini Devi Eye Hospital, Hyderabad, Telangana, India Purpose: The aim of this study was to describe the clinical features, treatment ...
Lodhi SA, Reddy JM, Peram V
core
PROBABLE VOGT-KOYANAGI-HARADA DISEASE: A CASE REPORT
, 2023 Vogt-Koyanagi-Harada(VKH)diseaseisabilateralgranulomatouspanuveitis affecting young adults, withor without systemic manifestations. The prognosis of VKH disease is generally favorable, however the development of complicationscanleadto ...
Elakhdari M. , Akannour Y. , Bardi C. , Mrad K. , Hassina S. , Serghini L. , El Hassan A. and Berraho A.
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Clinical Images: Syphilis as the great imitator; Behçet disease mimic
Arthritis &Rheumatology, Volume 78, Issue 2, Page 490-490, February 2026.
Ken Fukuda, Kenji Yamashiro
wiley +1 more source
Atypical Central Serous Chorioretinopathy
Türk Oftalmoloji Dergisi, 2017 Bullous central serous chorioretinopathy (CSCR) is a rare variant of CSCR characterized by severe serous retinal detachment which especially involves the inferior quadrants.
Zafer Cebeci +4 more
doaj +1 more source
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 +6 more
doaj
Case Reports in Ophthalmology, 2012 Purpose: To report 2 cases of Vogt-Koyanagi-Harada disease accompanied by remarkable choroidal folds in the acute stage. The early indicator of recurrence in these 2 cases was the identification of choroidal folds by spectral-domain optical coherence ...
Minoru Tanigawa +4 more
doaj +1 more source
Vogt-Koyanagi-Harada Disease in an Adolescent Boy
, 2014 Vogt-Koyanagi-Harada (VKH) disease is a rare multiorgan disorder that affects the melanocytes of the eyes, skin, inner ear, and meninges. It is more common in women and in patients 30 to 50 years of age; it is rarely seen in children. We report a 14-year-
Kaya, Kismet +2 more
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Fever, Headache, and Visual Blurring in a 17-Year-Old Woman. [PDF]
, 2004 Fever, Headache, and Visual Blurring in a 17-Year-Old ...
Sue Lightman (4941) +7 more
core +2 more sources
Frequency of Distinguishing Clinical Features in Vogt-Koyanagi-Harada disease
Ophthalmology (Rochester, Minn.), 2009 Purpose To determine the frequency of occurrence of limited clinical features which distinguish patients with Vogt-Koyanagi-Harada (VKH) disease from those with non-VKH uveitis. Design Comparative case series. Participants 1147 total patients.
N. Rao +11 more
semanticscholar +1 more source