Skip to main content
Figure 1 | BMC Medical Genetics

Figure 1

From: Inherited KIF21A and PAX6 gene mutations in a boy with congenital Fibrosis of extraocular muscles and aniridia

Figure 1

Phenotypes of the affected boy and his parents. (A) The pedigree, showing the boy inheriting CFEOM from his mother and aniridia from his father. (B) The boy and his mother, both of them with typical clinical features of CFEOM1. (C) The photo of the anterior segment in the left eye of the boy’s father, showing aniridia. (D) Aniridia in the left eye of the boy.

Back to article page