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  • Title: Sectoral iris heterochromia and retinal pigment variation in 13q-syndrome.
    Author: Kutzbach B, Mendelsohn N, Rath P, Summers CG.
    Journal: J AAPOS; 2007 Oct; 11(5):513-5. PubMed ID: 17933676.
    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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