Glaucoma, Congenital 646b13g 646b13g 646b13g 646b13g 646b13g 646b13g
General: Autosomal recessive; occurs more frequently in males; can occur isolated or associated with other systemic or ocular malformations (dysgenesis of iris, angle and peripheral cornea).
Ocular: Buphthalmos; corneal haze; glaucoma; epiphora.
Clinical: None.
Demenasis F. Further analysis of familial transmission of congenital glaucoma. Am J Hum Genet 1983; 35: 1156-l160.
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/.
Richt R, Shields B, Krupin T. The glaucomas. St. Louis: Mosby, 1989.
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