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J AAPOS. 2007 Oct;11(5):513-5.

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

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  • 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.

PMID:
17933676
[PubMed - indexed for MEDLINE]
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