Integrative analytical and statistical framework for optimization of multiplex qPCR detection of <i>TGFBI</i> mutations in refractive surgery candidates. [PDF]
J Zhejiang Univ Sci BGu Y +9 more
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A Review of the Use of Artificial Intelligence in Ophthalmology Imaging: Approximation to Ocular Histopathology. [PDF]
APMISHathaway JT, Stagner AM.
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The effect of cycloplegia on corneal power and diameter measured by an auto-kerato-refractometer in presbyopic patients with type 2 diabetes mellitus: a post-hoc analysis of a randomized clinical trial. [PDF]
BMC OphthalmolElmi Sadr N +3 more
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Characterization of superficial reticular corneal degeneration (a variant of band-shaped keratopathy) in eyes treated for retinopathy of prematurity. [PDF]
Indian J OphthalmolChaurasia S +3 more
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Nature Reviews Disease Primers, 2020 Corneal dystrophies are broadly defined as inherited disorders that affect any layer of the cornea and are usually progressive, bilateral conditions that do not have systemic effects.
Jodhbir S Mehta +2 more
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Degenerative or hereditary corneal diseases are sometimes difficult to discriminate. Corneal dystrophies affect approximately 0.09 % of the population. They are identified by the IC3D classification based on their phenotype, genotype and evidence gathered for their diagnosis.
Møller, Hans Ulrik, Lee, Barry
openaire +5 more sources
Fuchs’ Corneal Dystrophy [PDF]
Expert Review of Ophthalmology, 2010 Fuchs' corneal dystrophy (FCD) is a progressive, hereditary disease of the cornea first described a century ago by the Austrian ophthalmologist Ernst Fuchs. Patients often present in the fifth to sixth decade of life with blurry morning vision that increases in duration as the disease progresses.
Allen O Eghrari, John D Gottsch
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Biochemical Mechanisms of Aggregation in TGFBI-Linked Corneal Dystrophies [PDF]
Progress in Retinal and Eye Research, 2020 Transforming growth factor-β-induced protein (TGFBIp), an extracellular matrix protein, is the second most abundant protein in the corneal stroma. In this review, we summarize the current knowledge concerning the expression, molecular structure, binding ...
Lawrence Dedionisio +2 more
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Fuchs corneal dystrophy (FCD) is a hereditary, progressive disease of the posterior cornea which results in excrescences of Descemet membrane, endothelial cell loss, corneal edema, and, in late stages, bullous keratopathy. Structural changes are noted principally in Descemet membrane and the endothelium, with thickening of Descemet membrane, loss of ...
S Amer Riazuddin +2 more
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