FOXL2 belongs to the family of Forkhead transcription factors and is mutated in the Blepharophimosis Ptosis Epicanthus inversus Syndrome (BPES) [3], a genetic disorder characterized by eyelid malformations often associated with premature ovarian failure [4]. Here, FOXL2 is linked to blepharophimosis, ptosis, and epicanthus inversus syndrome.