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Hard and Soft Tissue Asymmetry in Patients with Skeletal Class III Malocclusion: A Cone-Beam Computed Tomography Study

This study aims to investigate hard and soft tissue asymmetry in skeletal Class III patients to elucidate how soft tissue thickness alters overall asymmetry and whether menton deviation is correlated with bilateral differences in hard and soft tissue prominence and soft tissue thickness. The cone-be...

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Autores principales: Tam, Tim King Man, Guo, Runzhi, Liu, Hao, Lin, Yifan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10000951/
https://www.ncbi.nlm.nih.gov/pubmed/36900013
http://dx.doi.org/10.3390/diagnostics13050869
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author Tam, Tim King Man
Guo, Runzhi
Liu, Hao
Lin, Yifan
author_facet Tam, Tim King Man
Guo, Runzhi
Liu, Hao
Lin, Yifan
author_sort Tam, Tim King Man
collection PubMed
description This study aims to investigate hard and soft tissue asymmetry in skeletal Class III patients to elucidate how soft tissue thickness alters overall asymmetry and whether menton deviation is correlated with bilateral differences in hard and soft tissue prominence and soft tissue thickness. The cone-beam computed tomography data of 50 skeletal Class III adults were divided based on menton deviation into symmetric (n = 25; deviation ≤ 2.0 mm) and asymmetric (n = 25; deviation > 2.0 mm) groups. Forty-four corresponding hard and soft tissue points were identified. Bilateral hard and soft tissue prominence and soft tissue thickness were compared using paired t-tests. The correlations between bilateral differences in these variables and menton deviation were examined using Pearson’s correlation analysis. In the symmetric group, no significant bilateral differences in soft and hard tissue prominence and soft tissue thickness were observed. In the asymmetric group, both hard and soft tissue prominence were significantly greater on the deviated side than the non-deviated side at most of the points; however, no significant differences in soft tissue thickness were detected except at point 9 (ST9/ST’9, p = 0.011). The difference of hard and soft tissue prominence at point 8 (H8/H’8 and S8/S’8) was positively correlated with menton deviation, whereas the soft tissue thickness at point 5 (ST5/ST’5) and point 9 (ST9/ST’9) was negatively correlated with menton deviation (p = 0.05). Soft tissue thickness does not affect overall asymmetry in the presence of underlying hard tissue asymmetry. Soft tissue thickness at the centre of the ramus may be correlated with the degree of menton deviation in patients with asymmetry; however, this correlation needs to be confirmed by further studies.
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spelling pubmed-100009512023-03-11 Hard and Soft Tissue Asymmetry in Patients with Skeletal Class III Malocclusion: A Cone-Beam Computed Tomography Study Tam, Tim King Man Guo, Runzhi Liu, Hao Lin, Yifan Diagnostics (Basel) Article This study aims to investigate hard and soft tissue asymmetry in skeletal Class III patients to elucidate how soft tissue thickness alters overall asymmetry and whether menton deviation is correlated with bilateral differences in hard and soft tissue prominence and soft tissue thickness. The cone-beam computed tomography data of 50 skeletal Class III adults were divided based on menton deviation into symmetric (n = 25; deviation ≤ 2.0 mm) and asymmetric (n = 25; deviation > 2.0 mm) groups. Forty-four corresponding hard and soft tissue points were identified. Bilateral hard and soft tissue prominence and soft tissue thickness were compared using paired t-tests. The correlations between bilateral differences in these variables and menton deviation were examined using Pearson’s correlation analysis. In the symmetric group, no significant bilateral differences in soft and hard tissue prominence and soft tissue thickness were observed. In the asymmetric group, both hard and soft tissue prominence were significantly greater on the deviated side than the non-deviated side at most of the points; however, no significant differences in soft tissue thickness were detected except at point 9 (ST9/ST’9, p = 0.011). The difference of hard and soft tissue prominence at point 8 (H8/H’8 and S8/S’8) was positively correlated with menton deviation, whereas the soft tissue thickness at point 5 (ST5/ST’5) and point 9 (ST9/ST’9) was negatively correlated with menton deviation (p = 0.05). Soft tissue thickness does not affect overall asymmetry in the presence of underlying hard tissue asymmetry. Soft tissue thickness at the centre of the ramus may be correlated with the degree of menton deviation in patients with asymmetry; however, this correlation needs to be confirmed by further studies. MDPI 2023-02-24 /pmc/articles/PMC10000951/ /pubmed/36900013 http://dx.doi.org/10.3390/diagnostics13050869 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Tam, Tim King Man
Guo, Runzhi
Liu, Hao
Lin, Yifan
Hard and Soft Tissue Asymmetry in Patients with Skeletal Class III Malocclusion: A Cone-Beam Computed Tomography Study
title Hard and Soft Tissue Asymmetry in Patients with Skeletal Class III Malocclusion: A Cone-Beam Computed Tomography Study
title_full Hard and Soft Tissue Asymmetry in Patients with Skeletal Class III Malocclusion: A Cone-Beam Computed Tomography Study
title_fullStr Hard and Soft Tissue Asymmetry in Patients with Skeletal Class III Malocclusion: A Cone-Beam Computed Tomography Study
title_full_unstemmed Hard and Soft Tissue Asymmetry in Patients with Skeletal Class III Malocclusion: A Cone-Beam Computed Tomography Study
title_short Hard and Soft Tissue Asymmetry in Patients with Skeletal Class III Malocclusion: A Cone-Beam Computed Tomography Study
title_sort hard and soft tissue asymmetry in patients with skeletal class iii malocclusion: a cone-beam computed tomography study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10000951/
https://www.ncbi.nlm.nih.gov/pubmed/36900013
http://dx.doi.org/10.3390/diagnostics13050869
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