dc.creatorFarah G.J.
dc.creatorFerreira G.Z.
dc.creatorSerra e Silva F.M.
dc.creatorMoraes M.D.
dc.date2010
dc.date2015-06-26T12:38:02Z
dc.date2015-11-26T14:58:27Z
dc.date2015-06-26T12:38:02Z
dc.date2015-11-26T14:58:27Z
dc.date.accessioned2018-03-28T22:10:10Z
dc.date.available2018-03-28T22:10:10Z
dc.identifier
dc.identifierRevista Portuguesa De Estomatologia, Medicina Dentaria E Cirurgia Maxilofacial. , v. 51, n. 1, p. 57 - 60, 2010.
dc.identifier16462890
dc.identifier10.1016/S1646-2890(10)70086-8
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-84871740364&partnerID=40&md5=0598fd7ac87a9479f654484618f5822f
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/91288
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/91288
dc.identifier2-s2.0-84871740364
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1255860
dc.descriptionThe aim of this article is go over the literature and describe a case of Ellis Van Creveld syndrome, in which the patient presented a neo-natal tooth Just-born and premature patient, female, came to the hospital of Limeira, São Paulo, and was attended by the Surgery and Maxillofacial Traumatology group from the Dentistry College of Piracicaba (FOPUNICAMP). Her main complaint was the neo-natal tooth. During the extraoral examination it was detected a tower shaped cranium, shortened limbs, lank and sparse hair, bilateral postaxial polydactyly, hypoplasic nails and heart changes. In the intraoral examination the signs included multiple labial frenum associated with gingival changes, and presence of a conic neo natal teeth. The diagnosis of Ellis van Creveld syndrome was based on the clinical and radiographic findings that included characteristics from Chondroectodermaldysplasia. It was not found any history of this syndrome in her family. Being thus, the Ellis Van Creveld Syndrome although rare, presents many characteristics that demand a multidiscipline treatment. Odontologic manifestations are there, that's why surgeons, especially dentists, must be aware of it so that their behavior can contribute for the patient well-being.
dc.description51
dc.description1
dc.description57
dc.description60
dc.descriptionPolymeropoulos, M.H., Ide, S.E., Wright, M., Goodship, J., Weissenbach, J., Pyeritz, R.E., Silva, D.E.O., Francomano, C.A., The gene for the Ellis-van Creveld syndrome is located on chromosome 4p16 (1996), 35, pp. 1-5. , GenomicsEllis, R.W., Crefeld, V.S., A syndrome characterized by ectodermaldysplasia, polydactyly, chondrodysplasia and congenital morbuscardia (1940) Arch Dis Child, 15, p. 65
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dc.descriptionKurian, K., Shanmugan, S., Vardat, H.T., Siddharth, G., Chondroecthodermal dysplasia (Ellis van Creveld syndrome): a report of three cases with review of literature (2007) Indian J Dent Res, 1, p. 18
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dc.descriptionSilva, D.E.O., Janovitz, D., Albuquerque, D.S.C., Ellis-van Creveld syndrome: report of 15 cases in an inbred kindred (1980) J Med Genet, 17, pp. 349-56
dc.descriptionAlvarez-borja, A., Ellis-Van Creveld syndrome. Report of two cases (1960) Pediatrics, 26, pp. 301-9
dc.descriptionPinto Jr., S.C., Lammel, C., Kim, J.H., Borges, J.L.P., Displasia condroectodérmica (síndrome de Ellis-van Creveld): relato de dois casos (2003) Rev Bras Ortop, 38, pp. 357-61
dc.descriptionWinter, L., Pediatric Orthopaedics, 4th ed (1996) Lippincott-Raven: Philadelphia
dc.languagept
dc.publisher
dc.relationRevista Portuguesa de Estomatologia, Medicina Dentaria e Cirurgia Maxilofacial
dc.rightsfechado
dc.sourceScopus
dc.titlePresença De Dente Neo-natal Em Portador Da Síndrome De Ellis Van-creveld: Relato De Caso
dc.typeArtículos de revistas


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