Results 161 to 170 of about 97,726 (210)
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Vestnik oftal'mologii, 2018
The article reviews modern clinical, morphological, and genetic aspects of corneal dystrophies based on the most recent international classification updated in 2015. Corneal dystrophies is a group of slow progressing, non-inflammatory corneal pathologies, most of which are characterized by variability of the associated traits.
S V, Trufanov +4 more
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The article reviews modern clinical, morphological, and genetic aspects of corneal dystrophies based on the most recent international classification updated in 2015. Corneal dystrophies is a group of slow progressing, non-inflammatory corneal pathologies, most of which are characterized by variability of the associated traits.
S V, Trufanov +4 more
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Archives of Ophthalmology, 1977
Fourteen members of four families with fleck systrophy of the corneal stroma were examined and studied. Corneal and lens changes were noted in all patients. Corneal sensation was normal. Corneal biopsies were performed on two patients and a corneal button of a patient with fleck dystrophy and keratoconus was studied.
J J, Purcell +2 more
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Fourteen members of four families with fleck systrophy of the corneal stroma were examined and studied. Corneal and lens changes were noted in all patients. Corneal sensation was normal. Corneal biopsies were performed on two patients and a corneal button of a patient with fleck dystrophy and keratoconus was studied.
J J, Purcell +2 more
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Corneal dystrophies and keratoconus
Current Opinion in Ophthalmology, 1995Knowledge about keratoconus (KC) and the corneal dystrophies continues to advance at a steady pace in view of the wide interest in these topics to basic scientists and clinical ophthalmologists. As in the past the articles on KC outnumber those on all of the other corneal dystrophies combined.
G K, Klintworth, T, Damms
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Histological Landmarks in Corneal Dystrophy: Pathology of Corneal Dystrophies
2011Corneal dystrophies are bilateral, progressive, genetically determined noninflammatory diseases restricted to the cornea. These are characterized by deposition of nonnative protein or other material, both intracellular and extracellular, within the corneal layers.
Geeta K, Vemuganti +2 more
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Corneal dystrophies and keratoconus
Current Opinion in Ophthalmology, 1996This year's reports have given us a better understanding of several dystrophies as well as improvements in diagnosis and treatment. Eight corneal dystrophies have now been mapped to specific chromosomes and of these lattice, granular, Avellino, and Reis Bückler's dystrophies map to the same region of chromosome 5q, raising the question whether they are
A J, Bron, Y S, Rabinowitz
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Archives of Ophthalmology, 1976
The clinical and histologic aspects of 34 primary and six reoperative keratoplasties for lattice corneal dystrophy are evaluated. Surgical and postoperative complications were minimal and not considered specific for lattice corneal dystrophy. Visual results were highly favorable in a long-term evaluation. No lattice figures were seen to recur in any of
J D, Lanier, M, Fine, B, Togni
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The clinical and histologic aspects of 34 primary and six reoperative keratoplasties for lattice corneal dystrophy are evaluated. Surgical and postoperative complications were minimal and not considered specific for lattice corneal dystrophy. Visual results were highly favorable in a long-term evaluation. No lattice figures were seen to recur in any of
J D, Lanier, M, Fine, B, Togni
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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
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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
openaire +2 more sources