Optic Atrophy, Nerve Deafness 858b14i 858b14i 858b14i 858b14i 858b14i
General: Autosomal recessive.
Ocular: Degeneration of optic nerves.
Clinical: Degeneration of the acoustic nerves; progressive polyneuropathy, distally.
Kollarits CR, et al. The autosomal dominant syndrome of progressive optic atrophy and congenital deafness. Am J Ophthalmol 1979; 87:789-792.
Konigsmark BW; Gorlin RJ. Genetic and metabolic deafness. Philadelphia: WB Saunders, 1976:108-l10.
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 Hoyt's Clinical Neuro-Ophthalmology. vol. 1, 4th ed. Baltimore: Williams & Wilkins, 1982:321.
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