Cataract, Microcornea Syndrome &nb 626i88g sp; &nb 626i88g sp; &nb 626i88g sp; &nb 626i88g sp; &nb 626i88g sp; &nb 626i88g sp; &nb 626i88g sp; &nb 626i88g sp; &nb 626i88g sp; &nb 626i88g sp; &nb 626i88g sp; &nb 626i88g sp; &nb 626i88g sp; &nb 626i88g sp; &nb 626i88g sp; &nb 626i88g sp; &nb 626i88g sp; &nb 626i88g sp; &nb 626i88g sp; &nb 626i88g sp; &nb 626i88g sp; &nb 626i88g sp; &nb 626i88g sp; &nb 626i88g sp; &nb 626i88g sp; &nb 626i88g sp; 211
General: Autosomal dominant; prominent in Sicilian families.
Ocular: Cataracts; microcornea; myopia.
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/.
Mellica F, et al. Autosomal dominant cataract and microcornea associated with myopia in a Sicilian family. Clin Genet 1985; 28:42-46.
Polomano RC, et al. Autosomal dominant cataracts and microcornea. Can J Ophthalmol 1979; 14:227-229.
Salmon JF, et al. Variable expressivity of autosomal dominant microcornea with cataract. Arch Ophthalmol 1988; 106:505-510.
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