Fig. 1From: Case report: a novel KERA mutation associated with cornea plana and its predicted effect on protein functionFamily with cornea plana. a. The pedigree is consistent with autosomal recessive inheritance; b. The right eye of patient IV:3, with a small, malformed pupil, and a hazy corneal limbus; c. The eyes of patient IV:4; d. The scalp of patient IV:4 at age 11, showing hypotrichosis on the anterior part of vertexBack to article page