Myelinated Optic Nerve Fibers
General: Autosomal dominant; transmiss 949b19j ion has been reported as autosomal recessive.
Ocular: White area adjacent to the disk caused by myelin sheath; pseudopapilledema.
Clinical: None.
Francois J. Heredity in Ophthalmology. St. Louis: CV Mosby, 1961:945.
Mann I. Developmental abnormalities of the eye, 2nd ed. Philadelphia: JB Lippincott, 1957.
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.
Ehlers-Danlos Syndrome (Fibrodysplasia Elastica Generalisata; Cutis Hyperelastica; Meekeren-Ehlers-Danlos Syndrome; Indian Rubber Man Syndro [...] |
Freeman-Sheldon Syndrome (Cranio-Carpo-Tarsal Dysplasia; Whistling Face Syndrome) 4 General: Rare; autosomal dominant and recessiv [...] |
Hodgkin Disease [...] |
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