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Sectoral iris heterochromia and retinal pigment variation in 13q-syndrome
Beth Kutzbach1, Nancy Mendelsohn, Pamela Rath
1Department of Pediatrics, University of Minnesota, Minneapolis, MN, USA.
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.
