نتایج جستجو برای: fuchs heterochromic iridocyclitis

تعداد نتایج: 2892  

Journal: :The British journal of ophthalmology 2002
T D Myers J R Smith A K Lauer J T Rosenbaum

BACKGROUND/AIM Iris nodules are an uncommon clinical sign in uveitis. The diseases most commonly associated with iris nodules and uveitis include sarcoidosis, Vogt-Koyanagi-Harada syndrome, multiple sclerosis, Fuchs' heterochromic iridocyclitis, and metastatic infection. While many of these diseases may be appropriately treated with immunosuppressive medication, the management of infectious uve...

Journal: :The British journal of ophthalmology 1987
L S Regenbogen N Naveh-Floman

We report a retrospective study of five patients with monocular Fuchs' heterochromic cyclitis associated with an ipsilateral Horner's syndrome. The minimum follow-up was 10 years. The presenting findings were cyclitis in three of the patients and heterochromia iridis associated with blepharoptosis in the other two. The major factors affecting all five patients were cataract and glaucoma. The in...

2005
Aize Kijlstra

Methods. Mature TGF-/?2 levels were determined in aqueous humor samples of 9 patients with Fuchs' heterochromic cyclitis, aqueous humor samples of 21 patients with other uveitis entities, and vitreous fluid samples of 19 patients with uveitis by using a commercially available sandwich ELISA. Total TGF-/?2 levels in ocular fluids were measured after heat activation. Aqueous humor samples from pa...

2002
T D Myers J T Rosenbaum

Background/aim: Iris nodules are an uncommon clinical sign in uveitis. The diseases most commonly associated with iris nodules and uveitis include sarcoidosis, VogtKoyanagi-Harada syndrome, multiple sclerosis, Fuchs’ heterochromic iridocyclitis, and metastatic infection. While many of these diseases may be appropriately treated with immunosuppressive medication, the management of infectious uve...

2015
Matthew D Benson Ian M MacDonald

INTRODUCTION Usher syndrome is a genetically heterogeneous condition and represents the most common cause of inherited combined vision and hearing loss. Deficits manifest as sensorineural hearing loss that typically develops at a young age and retinitis pigmentosa that can lead to peripheral vision loss and night blindness. As a result, this syndrome can have a significant impact on a patient's...

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