Iridogonodysgenesis (Iris Hypoplasia With Glaucoma)
General: Autosomal dominant; similar to Rieger syndrome or hereditary juvenile glaucoma.
Ocular: Stroma of iris hypoplastic; light irides; congenital glaucoma; optic atrophy; microphthalmia; opacities in Descemet membrane.
Clinical: None.
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/.
Pearce WG, et al. Autosomal dominant iridogonodysgenesis: a genetic and clinical study. Birth Defects 1982; 18: 561-569.
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