Sectoral iris heterochromia and retinal pigment variation in 13q-syndrome.
Journal: Journal Of AAPOS : The Official Publication Of The American Association For Pediatric Ophthalmology And Strabismus
Published:
Abstract
Chromosome 13q deletion syndrome is characterized by growth retardation, cognitive delays, and organ and musculoskeletal deformities. Typical ocular associations include retinoblastoma, microphthalmia, and colobomas. We report a case of bilateral iris heterochromia and retinal pigment abnormalities in a child with 13q-syndrome.
Authors
Beth Kutzbach, Nancy Mendelsohn, Pamela Rath, C Summers
Relevant Conditions