Skip to main content
Fig. 2 | BMC Ophthalmology

Fig. 2

From: Expanded phenotypic spectrum of FOXL2 Variant c.672_701dup revealed by whole-exome sequencing in a rare blepharophimosis, ptosis, and epicanthus inversus syndrome family

Fig. 2

Clinical features of the BPES-diagnosed family members. a Both the proband and the mother show bilateral ptosis and epicanthus inversus. Black arrow refers to lacquer cracks, peripapillary atrophy. b Blue arrow indicates macular patchy chorioretinal atrophy. The black arrow also points to lacquer cracks, peripapillary atrophy

Back to article page

BMC Ophthalmology

ISSN: 1471-2415

Contact us