Microphthalmos, Pigmentary Retinopathy, Glaucoma 646b18g 646b18g 646b18g
General: Autosomal dominant; three disorders combined.
Ocular: Microphthalmos; pigmentary retinopathy; glaucoma.
Clinical: None.
Hermann P. Syndrome: Microphthalmic-retinite pigmentaire-glaucoma. Arch Ophthalmol 1958; 18:17-24.
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/.
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