Cataract, Congenital or Juvenile (Cataract, Juvenile, Hutterite Type) 535e46f ; 535e46f ; 535e46f ; 535e46f ; 535e46f ; 535e46f ; 535e46f ; 535e46f ; 535e46f ; 535e46f ; 535e46f ; 205
General: Autosomal recessive; seen most frequently in people of Japanese origin; autosomal dominant inheritance also has been reported.
Ocular: Retinitis pigmentosa; Usher syndrome (retinitis pigmentosa and congenital deafness); congenital cataract of the 'i' phenotype; microphthalmos; keratoconus.
Clinical: Congenital deafness; galactokinase deficiency; epimerase deficiency.
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/.
Skokeir MHK, Lowry RB. Juvenile cataract in Hutterites. Am J Med Genet 1985; 22:495-500.
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