Reticular Pigmentary Retinal Dystrophy of Posterior Pole (Sjgren Disease)
General: Autosomal recessive; characterized by peculiar network of black-pigmented lines in poste 757i84h rior pole of retina.
Ocular: Fishnet-like knots on posterior pole of retina; drusen.
Clinical: None.
Deutman AF, et al. Reticular dystrophy of retinal pigment epithelium. Dystrophia reticularis laminae pigmentosae retinal of Sjogren. Arch Ophthalmol 1969; 82:4-9.
Deutman AF. Macular dystrophies. In: Ryan SJ, ed. Retina, vol. II, 2nd ed. St. Louis: Mosby, 1994:1216-l217.
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/.
Wocheslander E, et al. Die retikulare Pigment dystrophie nach Sjogren. Klin Monatsbl Augenheilkd 1980; 176:684.
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