Artículos de revistas
Presença De Dente Neo-natal Em Portador Da Síndrome De Ellis Van-creveld: Relato De Caso
Registro en:
Revista Portuguesa De Estomatologia, Medicina Dentaria E Cirurgia Maxilofacial. , v. 51, n. 1, p. 57 - 60, 2010.
16462890
10.1016/S1646-2890(10)70086-8
2-s2.0-84871740364
Autor
Farah G.J.
Ferreira G.Z.
Serra e Silva F.M.
Moraes M.D.
Institución
Resumen
The 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. 51 1 57 60 Polymeropoulos, 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 Goor, D., Rotem, Y., Friedman, A., Neufeld, H.N., Ellis-van Creveld syndrome in identical twins (1965) Br Heart J, 27, pp. 797-804 Keizer, D.P.R., Schilder, J.H., Ectodermal dysplasia, achondrodysplasia and congenital morbus cordis (1951) Am J Dis Child, 82, pp. 341-344 Mitchell, F.N., Waddell, W.W.Jr., Ellis-van Creveld syndrome: report of 2 cases in siblings (1958) Acta Paediatr, 47, pp. 142-151 Digilio, M., Marino, B., Ammirati, A., Borgaza, U., Giannotti, A., Dallapiccola, B., Cardiac malformations in patients with oral-facialskeletal syndromes: clinical similarities with heterotaxia (1999) Am J Med Genet, 84, pp. 350-356 Baujat, G., Merrer, L.M., Ellis-Van Creveld syndrome (2007) Orphanet Journal of Rare Diseases, 2, p. 27 Kurian, 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 Tachdjan, M., Pediatric Orthopaedics, 2a ed (1995) Manole:São Paulo Silva, 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 Alvarez-borja, A., Ellis-Van Creveld syndrome. Report of two cases (1960) Pediatrics, 26, pp. 301-9 Pinto 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 Winter, L., Pediatric Orthopaedics, 4th ed (1996) Lippincott-Raven: Philadelphia