dc.creatorMartelli, H
dc.creatorColetta, RD
dc.creatorMiranda, RT
dc.creatorde Barros, LM
dc.creatorSwerts, MS
dc.creatorBonan, PR
dc.date2009
dc.dateJUL
dc.date2014-07-30T18:03:45Z
dc.date2015-11-26T17:43:05Z
dc.date2014-07-30T18:03:45Z
dc.date2015-11-26T17:43:05Z
dc.date.accessioned2018-03-29T00:25:06Z
dc.date.available2018-03-29T00:25:06Z
dc.identifierMedicina Oral Patologia Oral Y Cirugia Bucal. Medicina Oral S L, v. 14, n. 7, n. E344, n. E348, 2009.
dc.identifier1698-4447
dc.identifierWOS:000270720800008
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/69775
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/69775
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1287491
dc.descriptionConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.descriptionTreacher Collins syndrome (TCS) is a rare autosomal dominant disorder of craniofacial development. Major features include midface hypoplasia, micrognathia, microtia, conductive hearing loss, and cleft palate. The present study is on the orofacial features of 7 Brazilian patients with sporadic TCS aged 4 to 38 years. All patients presented the typical down-slanting palpebral fissures, colobomas, zygomatic and mandibular hypoplasia, partial absence of the lower eyelid cilia, and abnormalities of the ears. Malocclusion was present in all patients, and an anterior open bite was found in 3 patients. None of the patients had a cleft palate.
dc.description14
dc.description7
dc.descriptionE344
dc.descriptionE348
dc.descriptionState Minas Gerais Research Foundation
dc.descriptionFundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG)
dc.descriptionConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.descriptionConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.languageen
dc.publisherMedicina Oral S L
dc.publisherValencia
dc.publisherEspanha
dc.relationMedicina Oral Patologia Oral Y Cirugia Bucal
dc.relationMed. Oral Patol. Oral Cir. Bucal
dc.rightsaberto
dc.sourceWeb of Science
dc.subjectTreacher Collins syndrome
dc.subjectorofacial features
dc.subjectgenetic disease
dc.subjectGene
dc.titleOrofacial features of Treacher Collins syndrome
dc.typeArtículos de revistas


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