Fuchs’ Heterochromic Iridocyclitis (FHI), also known as Fuchs’ uveitis syndrome (FUS), was first described in 1906 by Austrian ophthalmologist, Ernst Fuchs, who reported a series of 38 patients with iris heterochromia, cyclitis, and cataract.Since then, FHI has been further characterized as a constellation of clinical … See more Patients with FHI are often asymptomatic for many years prior to presentation as, unlike with other anterior uveitides, they typically will have no pain, redness, or photophobia. … See more Inflammation:Most cases of FHI do not require therapy, with patients generally having a good prognosis despite the persistent inflammation. The expected sequelae of chronic uveitis (posterior synechiae, persistent … See more Glaucoma is the most sight threatening and challenging complication of FHI. The prevalence of secondary glaucoma has been reported to be anywhere from 9-59% in FHI patients. As is … See more WebApr 19, 2024 · Fuchs' heterochromic cyclitis; Acquired Horner’s syndrome; Glaucoma and some medications used to treat it; Latisse, a repurposed glaucoma medication used cosmetically to thicken eyelashes; Pigment …
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WebAbstract. Fuchs' heterochromic iridocyclitis is a rare but significant cause of visual impairment. This form of uveitis is misdiagnosed more than any other in the entire field of uveitis. This is particularly true among brown-eyed individuals in whom gross heterochromia may not be diagnosed for many years. The clinical presentation of Fuchs ... WebGhost cell glaucoma is a clinical diagnosis. Diagnostic findings include presence of heme in the vitreous, ghost cells in the AC, delayed onset of increased intraocular pressure following vitreous hemorrhage, an open … hsa qualified plan
Ophthalmological Features of Leptospirosis - EyeWiki
WebFuchs' heterochromic iridocyclitis (FHI) is a chronic, low grade, usually unilateral, ocular inflammatory disease with a good visual prognosis. [eyewiki.org] Treatment and prognosis of secondary glaucoma in Fuchs’ heterochromic iridocyclitis. WebNov 27, 2024 · Fuchs syndrome is generally considered as an unilateral uveitis entity characterized by low-grade, non-granulomatous iridocyclitis, varying degrees of iris depigmentation, stellate or medium-sized keratic precipitates (KPs) diffusely distributed on the entire endothelium of the cornea [1,2,3].Vitreous opacity is common and retinal … WebAt the Howard Hughes Medical Institute, we believe in the power of individuals to advance science through research and science education, making discoveries that benefit … hsa reimbursement for prior year expense