Article
Molecular Studies of Tcf4 Gene and Correlation with Late‐Onset Fuchs Endothelial Corneal Dystrophy in the Greek Population: A Novel Cost‐Effective Diagnostic Algorithm
2025-10-08
Abstract excerpt
<h4>Background: </h4> /Aim: Late-onset Fuchs’ endothelial corneal dystrophy (FECD) is a hereditary, progressive, bilateral and irreversible disorder that is characterized by thickening of Descemet's membrane, microscopic collagenous protuberances known as guttae and accelerated loss of corneal endothelial cells. Patients initially complain of blurred vision and as the disease progresses, painful epithelial edema d...
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Identifiers and source
- Literature Corpus work
- 9f599ff9-984a-5025-a5c4-f5b64302ccf6
- DOI
- 10.20944/preprints202510.0544.v1
