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

Beth Kutzbach; Nancy Mendelsohn; Pamela Rath; C. Gail Summers

doi:10.1016/j.jaapos.2007.04.012

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

Beth Kutzbach, Nancy Mendelsohn, Pamela Rath, C. Gail Summers

Ophthalmology & Visual Neurosciences

Research output: Contribution to journal › Article › peer-review

8 Scopus citations

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.

Original language	English (US)
Pages (from-to)	513-515
Number of pages	3
Journal	Journal of AAPOS
Volume	11
Issue number	5
DOIs	https://doi.org/10.1016/j.jaapos.2007.04.012
State	Published - Oct 1 2007

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

Abstract

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