Cerebellar Ataxia, Cataract, Deafness, and Dementia or Psychosis (Heredopathia Ophthalmo-Oto-Encephalica) &nb 131i84b sp; &nb 131i84b sp; &nb 131i84b sp; &nb 131i84b sp; &nb 131i84b sp; &nb 131i84b sp; &nb 131i84b sp; &nb 131i84b sp; &nb 131i84b sp; &nb 131i84b sp; &nb 131i84b sp; &nb 131i84b sp; &nb 131i84b sp; &nb 131i84b sp; &nb 131i84b sp; &nb 131i84b sp; &nb 131i84b sp; &nb 131i84b sp; &nb 131i84b sp; &nb 131i84b sp; &nb 131i84b sp; &nb 131i84b sp; &nb 131i84b sp; &nb 131i84b sp; &nb 131i84b sp; &nb 131i84b sp; &nb 131i84b sp; &nb 131i84b sp; &nb 131i84b sp; &nb 131i84b sp; &nb 131i84b sp; &nb 131i84b sp; &nb 131i84b sp; &nb 131i84b sp; &nb 131i84b sp; 219
General: Autosomal dominant.
Ocular: Posterior polar cataracts.
Clinical: Tremor, paranoid psychosis; dementia; deafness.
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/.
Stromgren E. Heredopathia ophthalmo-oto-encephalica. Neurogenetic directory, part 1. Handbook Clin Neurol 1981; 42:150-l52.
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