Corneal Dystrophy, Meesmann Epithelial (Meesmann Epithelial Dystrophy of Cornea) 301
General: Autosomal dominant; rare; onset first year of life; possible that a disturbance of the cytoplasmic ground substance results in cellular homogenization with cyst formation.
Ocular: Myriads of fine punctate opacities in epithelium and Bowman membrane of cornea; thickening of the epithelial basement membrane of cornea; keratoconus.
Clinical: None.
Fine BS, et al. Meesmann's corneal dystrophy: ultrastructural features. Can J Ophthalmol 1982; 17:24.
Fine BS, et al. Meesmann's epithelial dystrophy of cornea. Am J Ophthalmol 1977; 83:633-642.
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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