Cataract, Nuclear (Coppock Cataract; Cataract, Discoid)& 212b19c nbsp; & 212b19c nbsp; & 212b19c nbsp; & 212b19c nbsp; & 212b19c nbsp; & 212b19c nbsp; & 212b19c nbsp; & 212b19c nbsp; & 212b19c nbsp; & 212b19c nbsp; & 212b19c nbsp; & 212b19c nbsp; & 212b19c nbsp; & 212b19c nbsp; & 212b19c nbsp; & 212b19c nbsp; 213
General: Autosomal dominant; epidemiologic evidence suggests that a single major gene can account for the correlation among siblings of nuclear sclerosis.
Ocular: Congenital zonular cataract; total nuclear cataract; fetal nucleus with scattered fine diffuse cortical opacities and incomplete cortical riders.
Clinical: None.
Harman NB. Congenital cataract: a pedigree of five generations. Trans Ophthalmol Soc U K 1909; 29:101-l08.
Heiba JM, et al. Genetic etiology of nuclear cataract: evidence for a major gene. Am J Med Genet 1993; 47:1208- 1214.
Lee JB, Benedict WL. Hereditary nuclear cataract. Arch Ophthalmol 1950; 44:643-650.
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/.
Merin S. Inherited cataracts. In: Merin S, ed. Inherited eye diseases. New York: Marcel Dekker, 1991:86-l20.
Melkersson-Rosenthal Syndrome (Melkersson Idiopathic Fibroedema; Miescher Cheilitis Granulomatosis) [...] |
Gorlin-Chaudhry-Moss Syndrome [...] |
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