Should Patients with Kearns -Sayre Syndrome and Corneal Endothelial Failure Be Genotyped for a TCF4 Trinucleotide Repeat,Commonly Associated with Fuchs Endothelial Corneal Dystrophy
The aim of this study was to describe the ocular phenotype in a case with Kearns-Sayre syndrome spectrum and to determine if corneal endothelial cell dysfunction could be attributed to other know distinct genetic causes.