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Orofacial features of Treacher Collins syndrome

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Orofacial features of Treacher Collins syndrome

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dc.contributor.author Martelli Júnior,Hercílio es
dc.contributor.author Della Coletta,Ricardo es
dc.contributor.author Miranda,Roseli Teixeira es
dc.contributor.author de Barros,Letízia Monteiro es
dc.contributor.author Swerts,Mário Sérgio Oliveira es
dc.contributor.author Bonan,Paulo Rogério Ferreti es
dc.date.accessioned 2023-06-22T12:12:38Z
dc.date.available 2023-06-22T12:12:38Z
dc.date.issued 2009 es
dc.identifier.citation Martelli-Júnior H, Coletta RD, Miranda RT , Barros LM, Swerts MS, Bonan PR. Orofacial features of Treacher Collins syndrome. Med Oral Patol Oral Cir Bucal. 2009 July 1;14(7):E344-E348. es
dc.identifier.uri https://hdl.handle.net/10550/88484
dc.description.abstract Treacher 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. es
dc.title Orofacial features of Treacher Collins syndrome es
dc.type journal article es_ES
dc.subject.unesco UNESCO:CIENCIAS MÉDICAS es
dc.type.hasVersion VoR es_ES
dc.identifier.url http://www.medicinaoral.com/medoralfree01/v14i7/medoralv14i7p344.pdf

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