Cataract, Floriform& 838g66i nbsp; & 838g66i nbsp; & 838g66i nbsp; & 838g66i nbsp; & 838g66i nbsp; & 838g66i nbsp; & 838g66i nbsp; & 838g66i nbsp; & 838g66i nbsp; & 838g66i nbsp; & 838g66i nbsp; & 838g66i nbsp; & 838g66i nbsp; & 838g66i nbsp; & 838g66i nbsp; & 838g66i nbsp; & 838g66i nbsp; & 838g66i nbsp; & 838g66i nbsp; & 838g66i nbsp; & 838g66i nbsp; & 838g66i nbsp; & 838g66i nbsp; & 838g66i nbsp; & 838g66i nbsp; & 838g66i nbsp; & 838g66i nbsp; & 838g66i nbsp; & 838g66i nbsp; & 838g66i nbsp; & 838g66i nbsp; & 838g66i nbsp; 209
General: Autosomal dominant; rare.
Ocular: Lens opacity takes the form of annular elements, arranged either independently or grouped together like petals of a flower; lenticonus; aniridia.
Clinical: None.
Doggart JH. Congenital cataract. Trans Ophthalmol Soc U K 1957; 77:31-37.
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/.
Noonan Syndrome (Male Turner Syndrome) 8 [...] |
Congenital Cataracts Facial Dysmorphism Neuropathy Syndrome &n [...] |
Bonnet-Dechaume-Blanc Syndrome (Cerebroretinal Arteriovenous Aneurysm Syndrome; Neuroretinoangiomatosis Syndrome; Wyburn-Mason Syndrome) [...] |
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? |