FOXL2 and blepharophimosis, ptosis, and epicanthus inversus syndrome: Autosomal dominant mutation of FOXL2 gene is also associated with blepharophimosis-ptosis-epicanthus-inversus syndrome (BPES) which manifests in two forms, BPES type II resulting in isolated craniofacial abnormalities and BPES type I additionally being accompanied by premature ovarian failure [91, 92].