Pseudopapilledema (Optic Nerve Head Drusen)
General: Autosomal dominant; incidence in males and females is approximately the same; two thirds of cases are bilateral; visual acuity usually unaffected; may cause slowly progressive visual field defect.
Ocular: Elevation of optic disk; drusen; injected conjunctiva; associated with retinitis pigmentosa, subretinal, subretinal pigment epithelium hemorrhages (rare).
Clinical: None.
Fite JD, Lewis AD. Family anomaly simulating papilledema: a case report. J Pediatr 1966; 68:927-931.
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, 1982:358.
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