Microphthalmos, Myopia, and Corectopia
General: Autosomal dominant; characterized by microphthalmos, myopia, and corectopia.
Ocular: Microphthalmos; myopia; corectopia; glaucoma; cataract; hypoplastic macula; spherophakia; microphakia.
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/.
Scheie HG. Text of Ophthalmology, 10th ed. Philadelphia: WB Saunders, 1986.
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