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Publicação:
Craniofacial Features in Richieri-Costa-Pereira Syndrome

dc.contributor.authorPardo, Milena P.
dc.contributor.authorSantos, Gabriela Lopes dos [UNESP]
dc.contributor.authorCarvalho, Izabel M.M.
dc.contributor.authorTjioe, Kellen Cristine [UNESP]
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.date.accessioned2022-04-29T08:29:11Z
dc.date.available2022-04-29T08:29:11Z
dc.date.issued2021-11-01
dc.description.abstractObjective: Patients with Richieri-Costa-Pereira syndrome (RCPS) present severe craniofacial alterations and frequently require orthodontic and surgical procedures. Thus, this study aims to describe the craniofacial relationships in patients with RCPS. Design: Panoramic radiographs and lateral cephalometric teleradiographs of 7 patients with RCPS and 7 age- and sex-matched nonsyndromic patients were analyzed. Cephalometric measurements were used to determine the size of apical bases, the relationship between them, the pattern of craniofacial growth, and the facial heights of the patients. Interobservers’ concordance was verified by intraclass coefficient. For comparison between the groups, paired t test was employed. P values <.05 indicated statistical significance. Results: Average age of patients with RCPS was 18.5 years. Six patients were female. All patients with RCPS had Pierre-Robin sequence while 2 also presented cleft mandible. Most patients with RCPS had missing lower central incisors (100%), lower lateral incisors (85.7%), lower second premolars (85.7%), and/or upper lateral incisors (57.1%). Concordance between observers was excellent for all cephalometric measurements (0.87-0.99). Patients with RCPS presented severe craniofacial alterations when compared to control group: sella–nasion–B point (SNB) angle (73.8o ± 4.86o vs 78.85o ± 4.53o, P =.029), maxillary length (7.89 cm ± 0.58 cm vs 16.36 cm ± 0.75 cm, P =.001), mandibular length (9.90 cm ± 0.46 cm vs 20.61 cm ± 0.45 cm, P =.001), upper anterior face height (5.41 cm ± 0.50 cm vs 9.40 cm ± 0.47 cm, P =.001), lower anterior face height (5.48 cm ± 0.75 cm vs 11.66 cm ± 0.55 cm, P =.001), and posterior face height (6.70 cm ± 0.33 cm vs 13.65 cm ± 1.06 cm, P =.001). There was no difference in SNB, A point–nasion–B point, pogonion–nasion–B point, and mandibular place angles between the groups (P >.05). Conclusion: Patients with RCPS present deficient development of maxilla and mandible when compared with nonsyndromic patients.en
dc.description.affiliationHospital for Rehabilitation of Craniofacial Anomalies University of São Paulo, Rua Silvio Marchione
dc.description.affiliationOral Oncology Center São Paulo State University, Rua Jose Bonifácio
dc.description.affiliationUnespOral Oncology Center São Paulo State University, Rua Jose Bonifácio
dc.format.extent1370-1375
dc.identifierhttp://dx.doi.org/10.1177/1055665620987749
dc.identifier.citationCleft Palate-Craniofacial Journal, v. 58, n. 11, p. 1370-1375, 2021.
dc.identifier.doi10.1177/1055665620987749
dc.identifier.issn1545-1569
dc.identifier.issn1055-6656
dc.identifier.scopus2-s2.0-85100544567
dc.identifier.urihttp://hdl.handle.net/11449/228900
dc.language.isoeng
dc.relation.ispartofCleft Palate-Craniofacial Journal
dc.sourceScopus
dc.subjectcephalometry
dc.subjectorthodontic treatment
dc.subjectorthognathic surgery
dc.subjectPierre-Robin sequence
dc.subjectRichieri-Costa-Pereira syndrome
dc.titleCraniofacial Features in Richieri-Costa-Pereira Syndromeen
dc.typeArtigo
dspace.entity.typePublication
unesp.author.orcid0000-0003-4145-0684[4]

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