Color Blindness, Blue-Mono-Cone Monochromatic Type &nb 111c21b sp; &nb 111c21b sp; &nb 111c21b sp; &nb 111c21b sp; &nb 111c21b sp; &nb 111c21b sp; &nb 111c21b sp; &nb 111c21b sp; &nb 111c21b sp; &nb 111c21b sp; &nb 111c21b sp; &nb 111c21b sp; &nb 111c21b sp; &nb 111c21b sp; &nb 111c21b sp; &nb 111c21b sp; &nb 111c21b sp; 269
General: Sex-linked; progressive.
Ocular: Total to partial color blindness; macular scar; poor central vision; poor color discrimination; infantile nystagmus; nearly normal retinal appearance in most cases; there is evidence showing alterations in the red and green visual pigment gene cluster.
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/.
Nathans J, et al. Molecular genetics of human blue cone monochromacy. Science 1989; 245:831-838.
Spivey BE. The X-linked recessive inheritance of atypical monochromatis. Arch Ophthalmol 1965; 74:327-333.
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