Fig. 3From: Novel FOXL2 mutations in two Chinese families with blepharophimosis-ptosis-epicanthus inversus syndromePictures representing the ocular defects of BPES patients from two Chinese families. Patients experience a combination of congenital eyelid anomalies: small palpebral fissures, ptosis, telecanthus, and epicanthus inversus. The left is Family (a) and the right is Family (b)Back to article page