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Nystagmus, congenital (congenital idiopathic nystagmus) 8


Nystagmus, Congenital (Congenital Idiopathic Nystagmus) 8

General: Autosomal dominant; pattern of inheritance in congenital nystagmus, whether of the 'motor' or 'sensory' type, may be autosomal dominant, recessive, or sex-linked.

Ocular: Vertical and horizontal nystagmus; this nystagmus occasionally is vertical or torsional; in addition, periodic alternating, downbeat, and see-saw nystagmus may be present at birth; normal electroretinogram.

Clinical: None.

Allen M. Three pedigrees of eye defects: primary hereditary nystagmus. Case study with genealogy. J Hered 1942; 33:454-456.

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/.

Miller NR, ed. Walsh and Hoyts Clinical Neuro-Ophthalmology, vol. 2, 4th ed. Baltimore: Williams & Wilkins, 1985:894.




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