Results 111 to 120 of about 406 (136)
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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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Schnyder's Crystalline Corneal Dystrophy
New England Journal of Medicine, 2010A 30-year-old Asian Indian woman with no medical history presented with blurry vision in both eyes. The patient reported that white spots in her eyes had been enlarging over the previous 9 years. Ophthalmologic examination revealed a corrected visual acuity of 20/50 in the right eye and 20/60 in the left eye.
Habeeb Ahmad, Martin Heur
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Phototherapeutic Keratectomy for Schnyder's Crystalline Corneal Dystrophy
Cornea, 2000To describe the treatment of Schnyder's crystalline dystrophy (SCD) with excimer laser phototherapeutic keratectomy (PTK).Chart review of three patients (four eyes) with SCD treated with PTK between March 1992 and December 1998. Pre- and posttreatment visual acuity, subjective glare, photophobia, manifest refraction, ultrasound pachymetry, hyperopic ...
L G, Paparo +5 more
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Unesterified Cholesterol in Schnyder's Corneal Crystalline Dystrophy
American Journal of Ophthalmology, 1987We examined a 51-year-old woman who had bilateral corneal crystalline deposits unassociated with xanthelasma or systemic involvement. Her son had similar corneal lesions. Plasma cholesterol and apolipoprotein A-I and B levels were normal in both patients.
M M, Rodrigues +3 more
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A Case of Schnyder Corneal Dystrophy with Crystals
Optometry and Vision Science, 2013ABSTRACT Purpose To report a rare corneal dystrophy and its common findings to help aid others in proper and early diagnosis and management. Case Report A 56‐year‐old male patient presented with the concern of blurry ...
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Phenotype–Genotype Correlation in Patients With Schnyder Corneal Dystrophy
Cornea, 2014The aim of this study was to analyze the corneal morphology features and define mutations in the UbiA prenyltransferase domain-containing 1 (UBIAD1) gene in patients with Schnyder corneal dystrophy from a Polish population.Five affected and 15 unaffected members originating from 3 families with Schnyder corneal dystrophy were included in the study ...
Nowinska, A. K. +10 more
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Fine mapping of the Schnyder?s crystalline corneal dystrophy locus
Human Genetics, 2004Schnyder's crystalline corneal dystrophy (SCCD) is a rare autosomal dominant eye disease with a spectrum of clinical manifestations that may include bilateral corneal clouding, arcus lipoides, and anterior corneal crystalline cholesterol deposition. We have previously performed a genome-wide linkage analysis on two large Swede-Finn families and mapped ...
Amanda M. Shearman +19 more
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Graefe's Archive for Clinical and Experimental Ophthalmology, 1989
Tight linkage was excluded for 8 markers in 37 blood relatives from 3 families, 29 of whom had granular corneal dystrophy (Groenouw I). Inconclusive results were obtained for linkage with four marker loci. The highest positive LOD score was 0.57 for linkage between glutamic pyruvic transaminase and granular corneal dystrophy. Tight linkage was excluded
J, Kömpf +4 more
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Tight linkage was excluded for 8 markers in 37 blood relatives from 3 families, 29 of whom had granular corneal dystrophy (Groenouw I). Inconclusive results were obtained for linkage with four marker loci. The highest positive LOD score was 0.57 for linkage between glutamic pyruvic transaminase and granular corneal dystrophy. Tight linkage was excluded
J, Kömpf +4 more
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Progress in molecular biology and translational science, 2016
The International Committee for Classification of Corneal Dystrophies (IC3D) provides updated data to ophthalmologists by incorporating traditional definitions of corneal dystrophies with new genetic, clinical, and pathologic information. Recent advances in the genetics of corneal dystrophies facilitate more precise classifications and elucidate each ...
Eung Kweon, Kim +2 more
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The International Committee for Classification of Corneal Dystrophies (IC3D) provides updated data to ophthalmologists by incorporating traditional definitions of corneal dystrophies with new genetic, clinical, and pathologic information. Recent advances in the genetics of corneal dystrophies facilitate more precise classifications and elucidate each ...
Eung Kweon, Kim +2 more
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[Schnyder's corneal dystrophy and hyperlipidemia (author's transl].
Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie. Albrecht von Graefe's archive for clinical and experimental ophthalmology, 1976Five out of ten members of a kinship were found to be affected by Schnyder's corneal dystrophy. Hyperlipoproteinemia was present in five out of eight cases examined (3 times type II, twice type IV). In one case with corneal dystrophy lipid levels were in the normal range, in another case, a child, hyperlipidemia was present without corneal ...
R, Kaden, G, Feurle
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