Grouped Pigmentation of the Macula 939b19j 939b19j 939b19j 939b19j 939b19j 939b19j 939b19j
General: Autosomal recessive.
Ocular: Grouped pigmentation limited to foveal area; metamorphopsia; pigmented spots around a clear hole in the foveal area.
Clinical: None.
Forsius H, et al. A genetic study of three rare retinal disorders: dystrophia retinae dysacusis syndrome, X-chromosomal retinoschisis and grouped pigments of the retina. Birth Defects 1971; 3:83-98.
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/.
Renardel de Lavalette, et al. Familial congenital grouped pigmentation of the retina. Am J Ophthalmol 1991; 112: 406-409.
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