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Patterns and frequency of keratoplasty in corneal dystrophy at a tertiary eye hospital in Nepal [PDF]
BMC OphthalmologyBackground Corneal dystrophy is a group of hereditary disorders with different presentations and management between regions and ethnic groups. This study aimed to report the patterns of corneal dystrophy, the frequency of keratoplasty requirement, and ...
Rachana Singh Rana +2 more
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Frontiers in Medicine, 2022 PurposeTo evaluate the value of artificial intelligence (AI) for recommendation of pupil dilation test using medical interview and basic ophthalmologic examinations.DesignRetrospective, cross-sectional study.SubjectsMedical records of 56,811 patients who
Hyunmin Ahn +7 more
doaj +1 more source
Frontiers in Medicine, 2022 PurposeTo assess the effects of femtosecond laser arcuate keratotomy with femtosecond laser-assisted cataract surgery in the management of corneal astigmatism, compared with conventional phacoemulsification cataract surgery.DesignRetrospective ...
Hyunmin Ahn +7 more
doaj +1 more source
Frontiers in Medicine, 2022 PurposeTo investigate an artificial intelligence (AI) model performance using multi-source anterior segment optical coherence tomographic (OCT) images in estimating the preoperative best-corrected visual acuity (BCVA) in patients with senile cataract ...
Hyunmin Ahn +7 more
doaj +1 more source
Corneal histomorphology and electron microscopic observation of R124L mutated corneal dystrophy in a relapsed pedigree [PDF]
International Journal of Ophthalmology, 2022 AIM: To investigate the histological characteristics and ultrastructure of recurrent Chinese R124L mutated corneal dystrophy after keratoplasty. METHODS: The subjects were enrolled from a Chinese family of corneal dystrophy with R124L heterozygous gene ...
Meng-Jun Fu +7 more
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Scientific Reports, 2021 We investigated the clinical and genetic features of patients with severe phenotype of granular corneal dystrophy type 2 (GCD2) associated with compound heterozygosity in the transforming growth factor-β-induced (TGFBI) gene.
Ikhyun Jun +5 more
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Genetic mutations and molecular mechanisms of Fuchs endothelial corneal dystrophy
Eye and Vision, 2021 Background Fuchs endothelial corneal dystrophy is a hereditary disease and the most frequent cause of corneal transplantation in the worldwide. Its main clinical signs are an accelerated decrease in the number of endothelial cells, thickening of Descemet’
Xuerui Liu +6 more
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American Journal of Ophthalmology Case Reports, 2022 Purpose: Phototherapeutic keratectomy (PTK) plays an important role in the management of Reis-Bucklers’ corneal dystrophy. The usage of PTK for the treatment of anterior corneal dystrophies is limited by the depth of ablation.
Gogri Pratik +3 more
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Diagnostic yield of candidate genes in an Australian corneal dystrophy cohort
Molecular Genetics & Genomic Medicine, 2022 Corneal dystrophies describe a clinically and genetically heterogeneous group of inherited disorders. The International Classification of Corneal Dystrophies (IC3D) lists 22 types of corneal dystrophy, 17 of which have been demonstrated to result from ...
Emmanuelle Souzeau +19 more
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Uncovering the profile of mutations of transforming growth factor beta-induced gene in Chinese corneal dystrophy patients [PDF]
International Journal of Ophthalmology, 2016 AIM: To uncover the mutations profile of transforming growth factor beta-induced (TGFBI) gene in Chinese corneal dystrophy patients and further investigate the characteristics of genotype-phenotype correlations.
Xiao-Dan Hao +4 more
doaj +1 more source