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Cataract, floriform   209


Cataract, Floriform& 838g66i nbsp;   & 838g66i nbsp;   & 838g66i nbsp;   & 838g66i nbsp;   & 838g66i nbsp;   & 838g66i nbsp;   & 838g66i nbsp;   & 838g66i nbsp;   & 838g66i nbsp;   & 838g66i nbsp;   & 838g66i nbsp;   & 838g66i nbsp;   & 838g66i nbsp;   & 838g66i nbsp;   & 838g66i nbsp;   & 838g66i nbsp;   & 838g66i nbsp;   & 838g66i nbsp;   & 838g66i nbsp;   & 838g66i nbsp;   & 838g66i nbsp;   & 838g66i nbsp;   & 838g66i nbsp;   & 838g66i nbsp;   & 838g66i nbsp;   & 838g66i nbsp;   & 838g66i nbsp;   & 838g66i nbsp;   & 838g66i nbsp;   & 838g66i nbsp;   & 838g66i nbsp;   & 838g66i nbsp;  209

General: Autosomal dominant; rare.

Ocular: Lens opacity takes the form of annular elements, arranged either independently or grouped together like petals of a flower; lenticonus; aniridia.

Clinical: None.

Doggart JH. Congenital cataract. Trans Ophthalmol Soc U K 1957; 77:31-37.

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/.




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