FOXL2 and blepharophimosis, ptosis, and epicanthus inversus syndrome: The FOXL2 mutations are linked to Blepharophimosis-Ptosis-Epicanthus Inversus syndrome (BPES) [126,127,128], adult ovarian granulosa-cell tumor [129], testicular adult-type granulosa cell tumors [130,131], ovarian Sertoli-Leydig cell tumors [132], incompletely differentiated sex cord-stromal tumors [131] and ovarian sex cord-stromal tumors [133] in human.