Results 171 to 180 of about 152,878 (215)
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Cornea, 2005
To report a case of a patient with a corneal band-shaped microcystic dystrophy.Case report.A 70-year-old woman with unilateral painless loss of visual acuity presented an epithelial feathery corneal opacification involving visual axis that showed an intraepithelial dense microcystic pattern.
Marco, Alvarez-Fischer +2 more
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To report a case of a patient with a corneal band-shaped microcystic dystrophy.Case report.A 70-year-old woman with unilateral painless loss of visual acuity presented an epithelial feathery corneal opacification involving visual axis that showed an intraepithelial dense microcystic pattern.
Marco, Alvarez-Fischer +2 more
openaire +2 more sources
Corneal dystrophies. II. Endothelial dystrophies
Survey of Ophthalmology, 1978In general, endothelial dystrophies present three types of clinical manifestations: 1) production of collagenous tissue posterior to Descemet's membrane which appears as cornea guttata, polymorphic excrescences or gray sheets; 2) a disrupted endothelial mosaic in specular reflection; and 3) corneal edema as a reflection of decreased endothelial barrier
G O, Waring +2 more
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The Genetics of the Corneal Dystrophies
2011Several comprehensive reviews have been written recently that summarize what is currently known about the molecular genetic basis of the corneal dystrophies. The one that is the current definitive reference on the subject is the IC3D classification of the corneal dystrophies, written by an international group of experts on the corneal dystrophies.
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Current Opinion in Ophthalmology, 2009
The present review of Schnyder corneal dystrophy (SCD) corrects the misconceptions in the published literature about this disease. Understanding the clinical findings facilitates diagnosis of the dystrophy.Retrospective case series of 115 affected individuals from 34 SCD families identified since 1989 reports the clinical findings in a large cohort and
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The present review of Schnyder corneal dystrophy (SCD) corrects the misconceptions in the published literature about this disease. Understanding the clinical findings facilitates diagnosis of the dystrophy.Retrospective case series of 115 affected individuals from 34 SCD families identified since 1989 reports the clinical findings in a large cohort and
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2022
Corneal dystrophies have classically referred to inherited, bilateral disease without systemic findings, although there are several exceptions to this definition. Hereditary pattern is not present in most patients with epithelial basement membrane dystrophy (EBMD).
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Corneal dystrophies have classically referred to inherited, bilateral disease without systemic findings, although there are several exceptions to this definition. Hereditary pattern is not present in most patients with epithelial basement membrane dystrophy (EBMD).
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Corneal Dystrophy and Paraproteinemia
American Journal of Ophthalmology, 1961J, FRANCOIS, M, RABAEY
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Ceska a slovenska oftalmologie : casopis Ceske oftalmologicke spolecnosti a Slovenske oftalmologicke spolecnosti, 2003
Authors concentrate on the occurrence of corneal hereditary dystrophies in the frame all pathology of the cornea in children age. They stress not rare appearance and pointed out on often diagnostic errors. They warn contemporary importance of long-time follow up of patients also in the adult age.
H, Stipanitzová, A, Gerinec
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Authors concentrate on the occurrence of corneal hereditary dystrophies in the frame all pathology of the cornea in children age. They stress not rare appearance and pointed out on often diagnostic errors. They warn contemporary importance of long-time follow up of patients also in the adult age.
H, Stipanitzová, A, Gerinec
openaire +1 more source
Fuchs Endothelial Corneal Dystrophy: The Vicious Cycle of Fuchs Pathogenesis
Progress in Retinal and Eye Research, 2021Adam Wylęgała +2 more
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