Three-dimensional comparison of mandibular morphology in young people with Treacher Collins syndrome and Pierre Robin sequence.


Journal

American journal of orthodontics and dentofacial orthopedics : official publication of the American Association of Orthodontists, its constituent societies, and the American Board of Orthodontics
ISSN: 1097-6752
Titre abrégé: Am J Orthod Dentofacial Orthop
Pays: United States
ID NLM: 8610224

Informations de publication

Date de publication:
Dec 2021
Historique:
received: 01 03 2020
revised: 08 05 2020
accepted: 01 06 2020
pubmed: 19 10 2021
medline: 26 11 2021
entrez: 18 10 2021
Statut: ppublish

Résumé

Treacher Collins syndrome (TCS) and nonsyndromic Pierre Robin sequence (PRS) share mandibular deficiency as a similar clinical finding. This study aimed to compare the mandibular size and morphology of subjects with TCS and PRS. Group TCS was composed of 17 subjects (7 male, 10 female) with a mean age of 11.5 years (standard deviation, 4.4) from a single center. Group PRS was composed of 17 subjects paired by age and sex with group TCS. Preorthodontic cone-beam computed tomography examinations of all patients were evaluated using Mimics Innovation Suite 17.0 (Materialise, Leuven, Belgium). Nine 3-dimensional measurements were performed in segmented 3D images of the mandible. Intragroup comparisons were performed using paired t tests. Intergroup comparisons were performed using analysis of variance and Tukey tests. The significance level considered was 5%. TCS showed a significant dimensional difference between less and more affected sides for ramus, condyles, and mandibular body. The mandibular dimensions in PRS were more symmetrical. Group TCS presented a smaller mandibular effective length and mandibular body length compared with PRS. The condyle width and height and the ramus width were also decreased in TCS. The gonial angle was greater in TCS compared with the PRS group. Young subjects with TCS presented a smaller, more vertical, and more asymmetrical mandible compared with nonsyndromic PRS.

Identifiants

pubmed: 34657764
pii: S0889-5406(21)00532-1
doi: 10.1016/j.ajodo.2020.06.053
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

835-843

Informations de copyright

Copyright © 2021. Published by Elsevier Inc.

Auteurs

Renata Mayumi Kato (RM)

Hospital for Rehabilitation of Craniofacial Anomalies, University of São Paulo, Bauru, Brazil. Electronic address: renata.mkato@gmail.com.

Priscila Padilha Moura (PP)

Department of Genetics, Hospital for Rehabilitation of Craniofacial Anomalies, University of São Paulo, Bauru, Brazil.

Roseli Maria Zechi-Ceide (RM)

Department of Genetics, Hospital for Rehabilitation of Craniofacial Anomalies, University of São Paulo, Bauru, Brazil.

Cristiano Tonello (C)

Hospital Department of Hospital for Rehabilitation of Craniofacial Anomalies, University of São Paulo, Bauru, Brazil.

Adriano Porto Peixoto (AP)

Department of Orthodontics, Hospital for Rehabilitation of Craniofacial Anomalies, University of São Paulo, Bauru, Brazil.

Daniela Garib (D)

Department of Orthodontics, Hospital for Rehabilitation of Craniofacial Anomalies, University of São Paulo, Bauru, Brazil; Bauru Dental School, University of São Paulo, Bauru, Brazil.

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Classifications MeSH