Results 41 to 50 of about 4,991,692 (213)
Vogt Koyanagi Harada disease following a recent COVID-19 infection
A 23-year-old female presented with a 3-day history of bilateral (OU) diminution of vision 3 weeks after COVID-19 infection. Best corrected visual acuity (BCVA) was 20/30 in right eye and 20/40 in left eye. Anterior segment showed OU 1+ cells in anterior
Eliza Anthony +3 more
semanticscholar +1 more source
Vogt–Koyanagi–Harada syndrome in the setting of COVID‐19 infection
To report a case of Vogt–Koyanagi–Harada disease (VKH) in a 27‐year‐old male 2 weeks proceeding COVID‐19 infection onset. Severe complications of VKH can be avoided by early diagnosis and adequate treatment with corticosteroids and immunosuppressants. It
Tiffany Eatz, Jude Hassan Charles
doaj +1 more source
Development and Evaluation of Diagnostic Criteria for Vogt-Koyanagi-Harada Disease
Importance To our knowledge, a set of well-defined diagnostic criteria is not yet developed for the diagnosis of Vogt-Koyanagi-Harada (VKH) disease. Objective To develop and evaluate a set of diagnostic criteria for VKH disease using data from Chinese ...
Peizeng Yang +26 more
semanticscholar +1 more source
Vogt-Koyanagi-Harada disease (VKH) is an important refractory uveitis mediated by pathological T cells (TCs). Tofacitinib (TOFA) is a JAK- targeted therapy for several autoimmune diseases.
Xiuxing Liu +10 more
semanticscholar +1 more source
Genetic landscape and autoimmunity of monocytes in developing Vogt–Koyanagi–Harada disease
Significance Vogt–Koyanagi–Harada (VKH) disease is one of the most common and severe vision-threatening autoimmune uveitis in Asians. However, the functional heterogeneity among subsets in human blood monocytes and the VKH disease-relevant populations ...
You-Jin Hu +12 more
semanticscholar +1 more source
Adalimumab in Vogt–Koyanagi–Harada disease: A case report
A 30-year-old Chinese woman presented to the ophthalmology department with bilateral blurry vision.; she was diagnosed with incomplete Vogt–Koyanagi–Harada (VKH).
Tingting Chen +3 more
doaj +1 more source
Uveo-Meningeal Syndromes: Vogt-Koyanagi-Harada (VKH) Disease
Ocular inflammatory symptoms with concurrent neuro-ophthalmologic manifestations can be diagnostically challenging. We provide a general overview of uveo-meningeal syndromes, which comprises a heterogeneous group of disorders that involve inflammation of
Rachana Haliyur, MD, PhD; Emily Cole, MD, MPH; Therese Sassalos, MD; Sangeeta Khanna, MD
core
Vogt-Koyanagi-Harada (VKH) disease is uncommon in the pediatric population and can have an aggressive course with serious visual sequelae. A 12-year-old Han Chinese American female, who presented with mild headaches and panuveitis with diffuse serous ...
Emily Su, Vikash S. Oza, Paul Latkany
doaj +1 more source
Uveitis associated with Vogt-Koyanagi-Harada (VKH) disease is a bilateral, chronic, granulomatous autoimmune disease associated with vitiligo, poliosis, alopecia, and meningeal and auditory manifestations.
A. A. Abu El-Asrar +3 more
semanticscholar +1 more source
Ocular syphilis mimicking Vogt–Koyanagi–Harada disease
The study aimed to present a case of ocular syphilis mimicking Vogt–Koyanagi–Harada (VKH) disease. This is an observational case report. A 59-year-old female with Sicca syndrome and rheumatoid arthritis presented to the ophthalmologic department with ...
Yu-Ching Lin +3 more
doaj +1 more source

