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Nonsyndromic Facial Asymmetry with Unilateral Condylar Aplasia
Introduction. The temporomandibular joint (TMJ) is the most complex elegantly designed joint in the human body. Abnormal development and growth of TMJ may lead to condyle aplasia present in several syndromes expressions, but it is extremely rare when not connected to any underlying pathological diso...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3759262/ https://www.ncbi.nlm.nih.gov/pubmed/24024045 http://dx.doi.org/10.1155/2013/631284 |
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author | Nallamothu, Ranganadh Kodali, Rama Mohan Koteswara Rao, N. Guttikonda, Leela krishna Vijayalakshmi, U. |
author_facet | Nallamothu, Ranganadh Kodali, Rama Mohan Koteswara Rao, N. Guttikonda, Leela krishna Vijayalakshmi, U. |
author_sort | Nallamothu, Ranganadh |
collection | PubMed |
description | Introduction. The temporomandibular joint (TMJ) is the most complex elegantly designed joint in the human body. Abnormal development and growth of TMJ may lead to condyle aplasia present in several syndromes expressions, but it is extremely rare when not connected to any underlying pathological disorder or in conjunction with any syndrome. Objective. A rare case of aplasia of the mandibular condyle is presented, along with 3D computed tomography (3D CT) findings. Conclusion. Based on clinical and radiological findings we suggest the abnormal development of the TMJ as the origin. The 3D CT has provided high-quality images, which made diagnosis and a prompt treatment plan possible. |
format | Online Article Text |
id | pubmed-3759262 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-37592622013-09-10 Nonsyndromic Facial Asymmetry with Unilateral Condylar Aplasia Nallamothu, Ranganadh Kodali, Rama Mohan Koteswara Rao, N. Guttikonda, Leela krishna Vijayalakshmi, U. Case Rep Dent Case Report Introduction. The temporomandibular joint (TMJ) is the most complex elegantly designed joint in the human body. Abnormal development and growth of TMJ may lead to condyle aplasia present in several syndromes expressions, but it is extremely rare when not connected to any underlying pathological disorder or in conjunction with any syndrome. Objective. A rare case of aplasia of the mandibular condyle is presented, along with 3D computed tomography (3D CT) findings. Conclusion. Based on clinical and radiological findings we suggest the abnormal development of the TMJ as the origin. The 3D CT has provided high-quality images, which made diagnosis and a prompt treatment plan possible. Hindawi Publishing Corporation 2013 2013-08-18 /pmc/articles/PMC3759262/ /pubmed/24024045 http://dx.doi.org/10.1155/2013/631284 Text en Copyright © 2013 Ranganadh Nallamothu et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Nallamothu, Ranganadh Kodali, Rama Mohan Koteswara Rao, N. Guttikonda, Leela krishna Vijayalakshmi, U. Nonsyndromic Facial Asymmetry with Unilateral Condylar Aplasia |
title | Nonsyndromic Facial Asymmetry with Unilateral Condylar Aplasia |
title_full | Nonsyndromic Facial Asymmetry with Unilateral Condylar Aplasia |
title_fullStr | Nonsyndromic Facial Asymmetry with Unilateral Condylar Aplasia |
title_full_unstemmed | Nonsyndromic Facial Asymmetry with Unilateral Condylar Aplasia |
title_short | Nonsyndromic Facial Asymmetry with Unilateral Condylar Aplasia |
title_sort | nonsyndromic facial asymmetry with unilateral condylar aplasia |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3759262/ https://www.ncbi.nlm.nih.gov/pubmed/24024045 http://dx.doi.org/10.1155/2013/631284 |
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