Análise tomográfica 3D da via áerea faríngea na Síndrome de Treacher Collins e sua relação com o padrão esquelético
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Tipo de documento: | Tese |
Idioma: | eng |
Título da fonte: | Biblioteca Digital de Teses e Dissertações da USP |
Texto Completo: | https://www.teses.usp.br/teses/disponiveis/61/61132/tde-20032020-161155/ |
Resumo: | Introduction: Treacher Collins syndrome (TCS) is a rare (1:50.000 live births) and severe anomaly of craniofacial development. It arises mainly from mutations in TCOF1 gene mapped at chromosome 5 and affects the development of first and second branchial arches. Maxillomandibular hypoplasia is among the main craniofacial characteristics. Objectives: This study aimed at investigating the skeletal craniofacial and pharyngeal morphologies of individuals with TCS, by means of cone beam computed tomography (CBCT) and to compare these data with those from a control population. Methods: CBCT scans of 26 individuals had the pharyngeal volume (V) and minimal cross-sectional area (mCSA) evaluated. The study group (TCS) was composed by CBCT scans of individuals (n=13) with TCS (7 males and 6 females; 20.2±4.7y). Control group (CG) was composed by CBCT scans of non-syndromic subjects (n=13) with the same type of skeletal pattern (2 males and 11 females; 26.6 ± 5.4y). Cephalometric data of maxillomandibular position, maxillomandibular dimensions and growth pattern were assessed. Statistics included Student t test and Pearson Correlation Coefficient (p 0.05). Results: Pharyngeal V and mCSA of TCS were smaller, although not significantly. Minimum CSA was located at the oropharyngeal level on the great majority of the cases. The jaws of TCS were significantly retropositioned and reduced, especially the mandible. It was observed a hiperdivergent growth pattern in TCS subjects. Conclusion: TCS is a skeletal class II high angle craniofacial malformation with reduced pharyngeal dimensions when compared with a control group. The micro and retrognathia seem to affect negatively the pharyngeal dimension of TCS population |
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Análise tomográfica 3D da via áerea faríngea na Síndrome de Treacher Collins e sua relação com o padrão esquelético3D tomographic analysis of the pharyngeal airways in Treacher Collins Syndrome and its relation with the skeletal patternCephalometryCleft palateCone-beam computed tomographyMandibulofacial dysostosisMicrognathismIntroduction: Treacher Collins syndrome (TCS) is a rare (1:50.000 live births) and severe anomaly of craniofacial development. It arises mainly from mutations in TCOF1 gene mapped at chromosome 5 and affects the development of first and second branchial arches. Maxillomandibular hypoplasia is among the main craniofacial characteristics. Objectives: This study aimed at investigating the skeletal craniofacial and pharyngeal morphologies of individuals with TCS, by means of cone beam computed tomography (CBCT) and to compare these data with those from a control population. Methods: CBCT scans of 26 individuals had the pharyngeal volume (V) and minimal cross-sectional area (mCSA) evaluated. The study group (TCS) was composed by CBCT scans of individuals (n=13) with TCS (7 males and 6 females; 20.2±4.7y). Control group (CG) was composed by CBCT scans of non-syndromic subjects (n=13) with the same type of skeletal pattern (2 males and 11 females; 26.6 ± 5.4y). Cephalometric data of maxillomandibular position, maxillomandibular dimensions and growth pattern were assessed. Statistics included Student t test and Pearson Correlation Coefficient (p 0.05). Results: Pharyngeal V and mCSA of TCS were smaller, although not significantly. Minimum CSA was located at the oropharyngeal level on the great majority of the cases. The jaws of TCS were significantly retropositioned and reduced, especially the mandible. It was observed a hiperdivergent growth pattern in TCS subjects. Conclusion: TCS is a skeletal class II high angle craniofacial malformation with reduced pharyngeal dimensions when compared with a control group. The micro and retrognathia seem to affect negatively the pharyngeal dimension of TCS populationIntroduction: Treacher Collins syndrome (TCS) is a rare (1:50.000 live births) and severe anomaly of craniofacial development. It arises mainly from mutations in TCOF1 gene mapped at chromosome 5 and affects the development of first and second branchial arches. Maxillomandibular hypoplasia is among the main craniofacial characteristics. Objectives: This study aimed at investigating the skeletal craniofacial and pharyngeal morphologies of individuals with TCS, by means of cone beam computed tomography (CBCT) and to compare these data with those from a control population. Methods: CBCT scans of 26 individuals had the pharyngeal volume (V) and minimal cross-sectional area (mCSA) evaluated. The study group (TCS) was composed by CBCT scans of individuals (n=13) with TCS (7 males and 6 females; 20.2±4.7y). Control group (CG) was composed by CBCT scans of non-syndromic subjects (n=13) with the same type of skeletal pattern (2 males and 11 females; 26.6 ± 5.4y). Cephalometric data of maxillomandibular position, maxillomandibular dimensions and growth pattern were assessed. Statistics included Student t test and Pearson Correlation Coefficient (p 0.05). Results: Pharyngeal V and mCSA of TCS were smaller, although not significantly. Minimum CSA was located at the oropharyngeal level on the great majority of the cases. The jaws of TCS were significantly retropositioned and reduced, especially the mandible. It was observed a hiperdivergent growth pattern in TCS subjects. Conclusion: TCS is a skeletal class II high angle craniofacial malformation with reduced pharyngeal dimensions when compared with a control group. The micro and retrognathia seem to affect negatively the pharyngeal dimension of TCS populationBiblioteca Digitais de Teses e Dissertações da USPSuedam, Ivy Kiemle TrindadeRibeiro, Alexandre de Almeida2019-05-17info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisapplication/pdfhttps://www.teses.usp.br/teses/disponiveis/61/61132/tde-20032020-161155/reponame:Biblioteca Digital de Teses e Dissertações da USPinstname:Universidade de São Paulo (USP)instacron:USPLiberar o conteúdo para acesso público.info:eu-repo/semantics/openAccesseng2024-10-09T13:16:04Zoai:teses.usp.br:tde-20032020-161155Biblioteca Digital de Teses e Dissertaçõeshttp://www.teses.usp.br/PUBhttp://www.teses.usp.br/cgi-bin/mtd2br.plvirginia@if.usp.br|| atendimento@aguia.usp.br||virginia@if.usp.bropendoar:27212024-10-09T13:16:04Biblioteca Digital de Teses e Dissertações da USP - Universidade de São Paulo (USP)false |
dc.title.none.fl_str_mv |
Análise tomográfica 3D da via áerea faríngea na Síndrome de Treacher Collins e sua relação com o padrão esquelético 3D tomographic analysis of the pharyngeal airways in Treacher Collins Syndrome and its relation with the skeletal pattern |
title |
Análise tomográfica 3D da via áerea faríngea na Síndrome de Treacher Collins e sua relação com o padrão esquelético |
spellingShingle |
Análise tomográfica 3D da via áerea faríngea na Síndrome de Treacher Collins e sua relação com o padrão esquelético Ribeiro, Alexandre de Almeida Cephalometry Cleft palate Cone-beam computed tomography Mandibulofacial dysostosis Micrognathism |
title_short |
Análise tomográfica 3D da via áerea faríngea na Síndrome de Treacher Collins e sua relação com o padrão esquelético |
title_full |
Análise tomográfica 3D da via áerea faríngea na Síndrome de Treacher Collins e sua relação com o padrão esquelético |
title_fullStr |
Análise tomográfica 3D da via áerea faríngea na Síndrome de Treacher Collins e sua relação com o padrão esquelético |
title_full_unstemmed |
Análise tomográfica 3D da via áerea faríngea na Síndrome de Treacher Collins e sua relação com o padrão esquelético |
title_sort |
Análise tomográfica 3D da via áerea faríngea na Síndrome de Treacher Collins e sua relação com o padrão esquelético |
author |
Ribeiro, Alexandre de Almeida |
author_facet |
Ribeiro, Alexandre de Almeida |
author_role |
author |
dc.contributor.none.fl_str_mv |
Suedam, Ivy Kiemle Trindade |
dc.contributor.author.fl_str_mv |
Ribeiro, Alexandre de Almeida |
dc.subject.por.fl_str_mv |
Cephalometry Cleft palate Cone-beam computed tomography Mandibulofacial dysostosis Micrognathism |
topic |
Cephalometry Cleft palate Cone-beam computed tomography Mandibulofacial dysostosis Micrognathism |
description |
Introduction: Treacher Collins syndrome (TCS) is a rare (1:50.000 live births) and severe anomaly of craniofacial development. It arises mainly from mutations in TCOF1 gene mapped at chromosome 5 and affects the development of first and second branchial arches. Maxillomandibular hypoplasia is among the main craniofacial characteristics. Objectives: This study aimed at investigating the skeletal craniofacial and pharyngeal morphologies of individuals with TCS, by means of cone beam computed tomography (CBCT) and to compare these data with those from a control population. Methods: CBCT scans of 26 individuals had the pharyngeal volume (V) and minimal cross-sectional area (mCSA) evaluated. The study group (TCS) was composed by CBCT scans of individuals (n=13) with TCS (7 males and 6 females; 20.2±4.7y). Control group (CG) was composed by CBCT scans of non-syndromic subjects (n=13) with the same type of skeletal pattern (2 males and 11 females; 26.6 ± 5.4y). Cephalometric data of maxillomandibular position, maxillomandibular dimensions and growth pattern were assessed. Statistics included Student t test and Pearson Correlation Coefficient (p 0.05). Results: Pharyngeal V and mCSA of TCS were smaller, although not significantly. Minimum CSA was located at the oropharyngeal level on the great majority of the cases. The jaws of TCS were significantly retropositioned and reduced, especially the mandible. It was observed a hiperdivergent growth pattern in TCS subjects. Conclusion: TCS is a skeletal class II high angle craniofacial malformation with reduced pharyngeal dimensions when compared with a control group. The micro and retrognathia seem to affect negatively the pharyngeal dimension of TCS population |
publishDate |
2019 |
dc.date.none.fl_str_mv |
2019-05-17 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/doctoralThesis |
format |
doctoralThesis |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://www.teses.usp.br/teses/disponiveis/61/61132/tde-20032020-161155/ |
url |
https://www.teses.usp.br/teses/disponiveis/61/61132/tde-20032020-161155/ |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
|
dc.rights.driver.fl_str_mv |
Liberar o conteúdo para acesso público. info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
Liberar o conteúdo para acesso público. |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.coverage.none.fl_str_mv |
|
dc.publisher.none.fl_str_mv |
Biblioteca Digitais de Teses e Dissertações da USP |
publisher.none.fl_str_mv |
Biblioteca Digitais de Teses e Dissertações da USP |
dc.source.none.fl_str_mv |
reponame:Biblioteca Digital de Teses e Dissertações da USP instname:Universidade de São Paulo (USP) instacron:USP |
instname_str |
Universidade de São Paulo (USP) |
instacron_str |
USP |
institution |
USP |
reponame_str |
Biblioteca Digital de Teses e Dissertações da USP |
collection |
Biblioteca Digital de Teses e Dissertações da USP |
repository.name.fl_str_mv |
Biblioteca Digital de Teses e Dissertações da USP - Universidade de São Paulo (USP) |
repository.mail.fl_str_mv |
virginia@if.usp.br|| atendimento@aguia.usp.br||virginia@if.usp.br |
_version_ |
1815256520920662016 |