Methemoglobinemia
General: Deficiency of enzyme; inherited or acquired, wit 313g66d h acquired most common; caused by contact with drugs and chemicals; disorder disappears when offending chemical is eliminated.
Ocular: Pigmentation of conjunctiva and retina.
Clinical: Cyanosis; mental retardation; central nervous system involvement.
Braunwald E, et al. Harrisons Principles of Internal Medicine, 11th ed. New York: McGraw-Hill, 1987.
Duke-Elder S, MacFaul PA. System of Ophthalmology, vol. XIII. St. Louis: CV Mosby, 1974.
Gibson QH. Methemoglobinemia-long ago and far away. Am J Hematol 1993; 42:3-6.
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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