Heterochromia Iridis 454e41e 454e41e 454e41e 454e41e 454e41e 454e41e 5
General: Autosomal dominant; can be associated with Horner, Waardenburg, and Marfan syndromes; may occur as an isolated phenomenon.
Ocular: Different pigmentation in the two irides or in the sectors of one iris (heterochromia iridium).
Clinical: None.
Gladstone RM. Development and significance of heterochromia of iris. Arch Neurol 1969; 21:184-l92.
McKusick VA. Mendelian Inheritance in Man; A Catalog of Human Genes and Genetic Disorders, 12th ed. Baltimore: The Johns Hopkins University Press, 1998.
Online Mendelian Inheritance in Man, OMIM. McKusick-Nathans Institute for Genetic Medicine, Johns Hopkins University and National Center for Biotechnology Information, National Library of Medicine, February 12, 2007. World Wide Web URL: https://www.ncbi.nlm.nih.gov/omim/.
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