Hereditary Microcornea, Glaucoma, and Absent Frontal Sinuses 5
General: Autosomal dominant. 353h72d
Ocular: Microcornea; glaucoma; epicanthal folds; optic cupping.
Clinical: Thickened palmar skin; torus palatinus; frontal sinus hypoplasia.
Holmes LB, Walton DS. Hereditary microcornea, glaucoma, and absent frontal sinuses; a family study. J Pediatr 1969; 74:968-971.
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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