Ellis-Van Creveld Syndrome. Case report and literature review
Mostra el registre complet de l'element
Visualització
(334.0Kb)
|
|
|
|
|
|
Alves Pereira,Daniela; Berini Aytés,Leonardo; Gay-Escoda,Cosme
|
|
Aquest document és un/a article, creat/da en: 2009
|
|
|
|
|
|
Ellis-van Creveld syndrome is a genetic disorder that was first described by Richard Ellis and Simon van Creveld in 1940. The four principal characteristics are chondrodysplasia, polydactyly, ectodermal dysplasia and congenital heart defects. The orofacial manifestations include multiple gingivolabial musculofibrous fraenula, dental anomalies, hypodontia and malocclusion. The disease can be diagnosed at any age, even during pregnancy. The differentiation should be made between Jeune syndrome and other orofaciodigital syndromes. |
|
Veure al catàleg Trobes
|
Aquest element apareix en la col·lecció o col·leccions següent(s)
Mostra el registre complet de l'element