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Oral manifestations of ellis-van creveld syndrome. A rare case report

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Oral manifestations of ellis-van creveld syndrome. A rare case report

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dc.contributor.author Peña Cardelles, Juan Francisco es
dc.contributor.author Domínguez-Medina, David A. es
dc.contributor.author Cano Durán, Jorge A. es
dc.contributor.author Ortega Concepción, Daniel es
dc.contributor.author Cebrián Carretero, José Luis es
dc.date.accessioned 2019-07-02T09:24:44Z
dc.date.available 2019-07-02T09:24:44Z
dc.date.issued 2019 es
dc.identifier.citation Peña Cardelles, Juan Francisco ; Domínguez-Medina, David A. ; Cano Durán, Jorge A. ; Ortega Concepción, Daniel ; Cebrián Carretero, José Luis. Oral manifestations of ellis-van creveld syndrome. A rare case report. En: Journal of Clinical and Experimental Dentistry, 11 3 2019: 290-295 es
dc.identifier.uri https://hdl.handle.net/10550/70638
dc.description.abstract Ellis-van Creveld syndrome (EVC) or chondroectodermal dysplasia is an autosomal recessive disorder, characterized by dwarfism, polydactyly, hypoplastic fingernails and congenital heart defects, finding in most of the cases orofacial anomalies. We describe a clinical case of a 9 year old male patient diagnosed with EVC who visited our Maxillofacial private consultation at Alcorcon Southern Hospital, presenting typical oral manifestations such as dental agenesis, delayed eruption, hypoplasia of the enamel, dental dysmorphism, taurodontism and supernumerary teeth. EVC syndrome is a rare disease and requires a multidisciplinary approach. Oral features are constant and requires the jointly performance of Odontologist and Maxillofacial surgeon aiming to get an appropriate treatment sequence surgery-orthodontics in order to achieve a suitable functional result to improve the quality of life of these patients. es
dc.title Oral manifestations of ellis-van creveld syndrome. A rare case report es
dc.type journal article es_ES
dc.subject.unesco UNESCO::CIENCIAS MÉDICAS es
dc.identifier.doi 10.4317/jced.55543 es
dc.type.hasVersion VoR es_ES

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