SLC4A11 and Fuchs endothelial corneal dystrophy: Moreover, SLC4A11 was identified to be responsible for three corneal endothelial dystrophies, recessive congenital hereditary endothelial dystrophy (CHED2) [8], late onset Fuchs endothelial dystrophy (FECD) [9], and corneal dystrophy with perceptive deafness (Harboyan syndrome) [10].