Keratitis Fugax Hereditaria 727g62h 727g62h 727g62h 727g62h 727g62h 6
General: Autosomal dominant; onset from age 4 to 12 years; characterized by acute attacks of keratitis.
Ocular: Keratitis; corneal opacities.
Clinical: None.
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/.
Valle O. Keratitis fugax hereditaria. Duodecim 1964; 80:659-664.
Martsolf Syndrome [...] |
Macular Dystrophy, Fenestrated Sheen Type General: Aut [...] |
Carpenter Syndrome (Acrocephalopolysyndactyly Type II) [...] |
Copyright © 2010 - 2024
: eSanatos.com - Reproducerea, chiar si partiala, a materialelor de pe acest site este interzisa!
Informatiile medicale au scop informativ si educational. Ele nu pot inlocui consultul medicului si nici diagnosticul stabilit in urma investigatiilor si analizelor medicale la un medic specialist.
Termeni si conditii - Confidentialitatea datelor - Contact
Despre diseases |
| Alte sectiuni |
|
Ai o problema medicala? |
