Sectoral iris heterochromia and retinal pigment variation in 13q-syndrome.

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. 

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Cite this paper

@article{Kutzbach2007SectoralIH, title={Sectoral iris heterochromia and retinal pigment variation in 13q-syndrome.}, author={Beth R Kutzbach and Nancy J. Mendelsohn and Pamela P Rath and Courtney Summers}, journal={Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus}, year={2007}, volume={11 5}, pages={513-5} }