Sequência De Pierre Robin - Etiopatogenia, Características Clínicas E Formas De Tratamento

dc.creatorSato F.R.L.
dc.creatorSetten K.C.
dc.creatorSverzut A.T.
dc.creatorde Moraes M.
dc.creatorMoreira R.W.F.
dc.date2007
dc.date2015-06-30T18:52:08Z
dc.date2015-11-26T14:39:05Z
dc.date2015-06-30T18:52:08Z
dc.date2015-11-26T14:39:05Z
dc.date.accessioned2018-03-28T21:44:32Z
dc.date.available2018-03-28T21:44:32Z
dc.identifier
dc.identifierRevista Portuguesa De Estomatologia, Medicina Dentaria E Cirurgia Maxilofacial. , v. 48, n. 3, p. 161 - 166, 2007.
dc.identifier16462890
dc.identifier10.1016/S1646-2890(07)70135-8
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-84863665200&partnerID=40&md5=2a6f62a690b09acb0269acfaf9583b0a
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/105158
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/105158
dc.identifier2-s2.0-84863665200
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1249855
dc.descriptionNewborns with Pierre-Robin sequence often suffer from serious or even life-threatening obstructions in the respiratory tract resulting from anatomic malformations (micrognathia, glossoptosis and potentially a median cleft palate). Such babies require immediate effective therapeutic measures. Based on these facts, the aim of this article was to make a review of the literature about the etiopathogenesis, clinical characteristics and the current treatments for theses structural alterations.
dc.description48
dc.description3
dc.description161
dc.description166
dc.descriptionLannelongue, R., Menard, V., Traite des Affections Congenitales (1891) Paris: Asselin et Houzeau, p. 264
dc.descriptionRobin, P., Glossoptosis due to atresia and hypotrophy of the mandible (1934) Am J Dis Chilf, 48, pp. 541-547
dc.descriptionElliott, M.A., Studen-Pavlovich, D.A., Ranalli, D.N., Prevalence of selected pediatric conditions in children with Pierre Robin sequence (1995) Pediatr Dent, 17, pp. 106-111
dc.descriptionCocke Jr., W., Experimental production of micrognathia and glossoptosis associated with cleft palate (Pierre Robin syndrome) (1966) Plast Reconstr Surg, 38, pp. 395-403
dc.descriptionPoswillo, D., The aetiology and surgery of cleft palate with micrognathia (1968) Ann R Coll Surg Engl, 43, pp. 61-88
dc.descriptionPoswillo, D., The aetiology and surgery of cleft palate with micrognathia (1968) Ann R Coll Surg Engl, 43, pp. 61-88
dc.descriptionLatham, R.A., The pathogenesis of cleft palate associated with the Pierre Robin syndrome An analysis of a seventeenweek human foetus (1966) Br J Plast Surg, 19, pp. 205-214
dc.descriptionBecker, R., Palm, D., Zur kausalen und fonnalen genese des Pierre Robin syndroms (1966) Dtsch Zahnärzth Z, 21, pp. 1321-1338
dc.descriptionRintala, A., Ranta, R., Stegars, T., On the pathogenesis of cleft palate in the Pierre Robin syndrome (1984) Scand J Plast Reconstr Surg, 18, pp. 237-240
dc.descriptionEdwards, J.R., Newall, D.R., The Pierre Robin syndrome reassessed in the light of recent research (1985) Br J Plast Surg, 38, pp. 339-342
dc.descriptionCohen Jr., M.M., (1982) The Child with Multiple Birth Defects, , New York: Raven Press
dc.descriptionCohen Jr., M.M., The. Robin anomalad: its nonspecific, and associated syndromes (1976) J Oral Surg, 34, pp. 587-593
dc.descriptionLewis, M.B., Pashayan, H.M., Management of infants with Robin anomaly (1980) Clin Pediatr, 19, pp. 519-521
dc.descriptionSmith, D.W., Classification, nomenclature and meaning of morphologic defects (1975) J Pediatr, 87, p. 162
dc.descriptionGorlin, R.J., Cohen, M.M., Hennekam, R.C.M., (2001) Syndromes of the Head and Neck, , 4a ed. Oxford: Oxford University Press
dc.description(1994), OMS., Classificação Internacional das Doenças -, CID., 10., 1a, ed., São Paulo: EduspFraser, F.C., Trasler, D.G., Walker, B.E., Fraser, F.C., Congenital malformations produced by amniotic sac puncture (1956) Science, 124 (124), p. 439
dc.descriptionWalker, B.E., Effects on palate development of mechanical interference with the fetal environment (1959) Science, 130, p. 981
dc.descriptionHarris, J.W.S., Oligohydramnios and costisone induced cleft palate (1964) Nature, 203, p. 5334
dc.descriptionSheffield, L.J., Reiss, J.A., Strohm, Y., Gildin, M., A genetic follow up study of 64 patients with the Pierre Robin complex (1987) Am J Med Genet, 28, pp. 25-36
dc.descriptionCarroll, D.B., Peterson, R.A., Worton, E.W., Birnbaum, L.M., Hereditary factor in the Pierre Robin syndrome (1971) Br J Plast Surg, 24, pp. 43-47
dc.descriptionLapage, C.P., Micrognathia in the new-born (1937) Lancet, 1, pp. 323-324
dc.descriptionSmith, J.L., Stowe, F.R., The Pierre Robin syndrome: a review of 39 cases with mphasis on associated ocular lesions (1961) Pediatrics, 27, pp. 128-133
dc.descriptionSachtleben, P., Zur pathogenese und therapie des Pierre Robin syndrome (1964) Arch Kinderheilk, 171, pp. 55-63
dc.descriptionTan, I.K.L., The Pierre Robin syndrome (1968) J Singapore Paediatr Soc, 10, pp. 88-94
dc.descriptionMarques, I.L., Barbieri, M.A., Bettiol, H., Etiopathogenesis of isolated Robin sequence (1998) Cleft Palate Craniofac J, 35, pp. 517-525
dc.descriptionVegter, F., Hage, J.J., Mulder, J.W., Pierre Robin syndrome: mandibular growth during the first year of life (1999) Ann Plast Surg, 42, pp. 154-157
dc.descriptionGruen, P.M., Carranza, A., Karmody, C.S., Bachor, E., Anomalies of the ear in the Pierre Robin triad (2005) Ann Otol Rhinol Laryngol, 114, pp. 605-613
dc.descriptionMarques, I.L., Sousa, T.V., Carneiro, A.F., Peres, S.P.B., Barbieri, M.A., Bettiol, H., Seqüência de Robin - Protocolo Único de Tratamento (2005) J Pediatr (Rio J), 81, pp. 4-22
dc.descriptionSher, A.E., Mechanisms of airway obstruction in Robin sequence: implications for treatment (1992) Cleft Palate Craniofac J, 29, pp. 224-231
dc.descriptionMarques, I.L., Sousa, T.V., Carneiro, A.F., Barbieri, M.A., Bettiol, H., Gutierrez, M.R., Clinical experience with infants with Robin sequence: a prospective study (2001) Cleft Palate Craniofac J, 38, pp. 171-178
dc.descriptionHamdi, M., Brutus, J.P., Mey, D., Clinical experience with Pierre Robin sequence (2004) Eur J Plast Surg, 26, pp. 401-405
dc.descriptionCruz, M.J., Kerschner, J.E., Beste, D.J., Conley, S.F., Pierre Robin sequences: secondary respiratory difficulties and intrinsic feeding abnormalities (1999) Laryngoscope, 109, pp. 1632-1636
dc.descriptionDouglas, B., The treatment of micrognathia with obstruction by a plastic procedure (1964) Plast Reconstr Surg, 1, pp. 300-308
dc.descriptionArgamso, R.V., Glossopexy for upper airway obstruction in Robin sequence (1992) Cleft Palate Craniofac J, 29, pp. 232-238
dc.descriptionCaouette-Laberge, L., Bayet, B., Larocque, Y., The Pierre Robin sequence: review of 125 cases and evolution of treatment modalities (1994) Plast Reconstr Surg, 93, pp. 934-942
dc.descriptionSinger, L.T., Kercsmar, C., Legris, G., Orlowski, J.P., Hill, B.P., Doershuk, C., Developmental sequelae of long-term infant tracheostomy (1989) Dev Med Child Neurol, 31, pp. 224-230
dc.descriptionLudwig, B., Glasl, B., Sader, R., Schopf, P., Conservative Orthodontic Primary Care of Four Newborn with Pierre-Robin Sequence Triad (2007) J Orofac Orthop, 68, pp. 56-61
dc.descriptionSalmon, M.A., Developmental defects and syndromes (1978) Aylesbury: HMM;
dc.descriptionBush, P.G., Williams, A.J., Incidence of the Robin anomalad (Pierre Robin syndrome) (1983) Br J Plast Surg, 36, pp. 434-437
dc.languagept
dc.publisher
dc.relationRevista Portuguesa de Estomatologia, Medicina Dentaria e Cirurgia Maxilofacial
dc.rightsfechado
dc.sourceScopus
dc.titleSequência De Pierre Robin - Etiopatogenia, Características Clínicas E Formas De Tratamento
dc.typeArtículos de revistas


Este ítem pertenece a la siguiente institución