Variants
Sign InSign Up

Corneal dystrophy, Fuchs endothelial, 6

Your Results

Sign In

Description

Fuchs endothelial corneal dystrophy (FECD) is the most common genetic disorder of the corneal endothelium. Late-onset FECD is marked by thickening of Descemets membrane and excrescences, called guttae, that typically appear in the fourth or fifth decade. Disease progression results in decreased visual acuity as a result of increasing corneal edema, and end-stage disease is marked by painful epithelial bullae (summary by Riazuddin et al., 2013). For a discussion of genetic heterogeneity of Fuchs endothelial corneal dystrophy, see FECD1 (136800).

OMIM

  • Mode of Inheritance

    VARIANTS

    2

    SEE THE VARIANTS →

    Genes

    External Links

    • OMIM

      613270

    • Orphanet
    • HPO
    • Medgen

      C2750448

    © 2024 Biocodify. All rights reserved.

    TwitterTwitter

    Product

    HomePricingDashboard

    Stay up to date

    The latest news and updates from Biocodify, sent to your inbox.