Cranial Nerves, Recurrent Paresis 121g65b 121g65b 121g65b 121g65b 121g65b 121g65b 121g65b 121g65b 121g65b 121g65b 121g65b 121g65b 121g65b 121g65b 121g65b 121g65b 121g65b 121g65b 121g65b 121g65b 121g65b 121g65b 121g65b 121g65b 121g65b 121g65b 309
General: Autosomal recessive; rare, recurrent episodes of Bell palsy and external ophthalmoplegia; lack of iridoplegia distinguishes it from aneurysm.
Ocular: External ophthalmoplegia; third nerve palsy.
Clinical: Bell palsy; diabetes; polycythemia.
Currie S. Familial oculomotor palsy with Bell's palsy. Brain 1980; 93: 193-l98.
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/.
Epiphyseal Dysplasia of Femoral Heads, Myopia, Deafness General: Autosomal r [...] |
Ultraviolet Radiation 1 [...] |
X X Chromosomal Deletion [...] |
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? |
