dc.creatorPerez, D E C
dc.creatorPereira Neto, J S
dc.creatorGraner, E
dc.creatorLopes, M A
dc.date2005-Mar
dc.date2015-11-27T13:01:57Z
dc.date2015-11-27T13:01:57Z
dc.date.accessioned2018-03-29T01:00:34Z
dc.date.available2018-03-29T01:00:34Z
dc.identifierInternational Journal Of Paediatric Dentistry / The British Paedodontic Society [and] The International Association Of Dentistry For Children. v. 15, n. 2, p. 131-5, 2005-Mar.
dc.identifier0960-7439
dc.identifier10.1111/j.1365-263X.2005.00595.x
dc.identifierhttp://www.ncbi.nlm.nih.gov/pubmed/15790372
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/196199
dc.identifier15790372
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1296432
dc.descriptionSturge-Weber syndrome is a congenital disorder characterized by vascular facial birthmarks and neurological abnormalities. Oral cavity involvement may occur, and the extent of the vascular abnormality may vary considerably. The present authors report the case of a 6-year-old girl with Sturge-Weber syndrome, focusing on the clinical and radiographic features. Her dental management involved a multidisciplinary team and included orthodontic treatment using removable appliances.
dc.description15
dc.description131-5
dc.languageeng
dc.relationInternational Journal Of Paediatric Dentistry / The British Paedodontic Society [and] The International Association Of Dentistry For Children
dc.relationInt J Paediatr Dent
dc.rightsfechado
dc.rights
dc.sourcePubMed
dc.subjectAnodontia
dc.subjectBicuspid
dc.subjectCephalometry
dc.subjectChild
dc.subjectFemale
dc.subjectFollow-up Studies
dc.subjectHumans
dc.subjectMalocclusion
dc.subjectOpen Bite
dc.subjectSturge-weber Syndrome
dc.titleSturge-weber Syndrome In A 6-year-old Girl.
dc.typeArtículos de revistas


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