Systematic review of SLC4A11, ZEB1, LOXHD1, and AGBL1 variants in the development of Fuchs’ endothelial corneal dystrophy

Systematic review of SLC4A11, ZEB1, LOXHD1, and AGBL1 variants in the development of Fuchs’ endothelial corneal dystrophy

IntroductionThe pathogenic role of variants in TCF4 and COL8A2 in causing Fuchs’ endothelial corneal dystrophy (FECD) is not controversial and has been confirmed by numerous studies. The causal role of other genes, SLC4A11, ZEB1, LOXHD1, and AGBL1, which have been reported to be associated with FECD...

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Bibliographic Details
Main Authors: Tatiana Romanovna Tsedilina, Elena Sharova, Valeriia Iakovets, Liubov Olegovna Skorodumova
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-06-01
Series:Frontiers in Medicine
Subjects:
Fuchs dystrophy
SLC4A11
ZEB1
LOXHD1
AGBL1
posterior polymorphous corneal dystrophy type 3
Online Access:https://www.frontiersin.org/articles/10.3389/fmed.2023.1153122/full

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https://www.frontiersin.org/articles/10.3389/fmed.2023.1153122/full

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