Cataract, Microphthalmia and Nystagmus 747c27h ; 747c27h ; 747c27h ; 747c27h ; 747c27h ; 747c27h ; 747c27h ; 747c27h ; 747c27h ; 747c27h ; 747c27h ; 747c27h ; 747c27h ; 747c27h ; 747c27h ; 747c27h ; 747c27h ; 747c27h ; 747c27h ; 747c27h ; 747c27h ; 747c27h ; 747c27h ; 212
General: Autosomal recessive.
Ocular: Miosis; cataract; nystagmus; microphthalmia.
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/.
Temtamy SA, Shalach BA. Genetic heterogeneity of the syndrome: microphthalmos with congenital cataract. Birth Defects 1974; 10:292-293.
Zeiter HJ. Congenital microphthalmos: a pedigree of 4 affected siblings and an additional report of 44 sporadic cases. Am J Ophthalmol 1963; 55:910-922.
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