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Isolated Congenital Camptodactyly and Temporomandibular Joint Articular Disc Displacement

The development of craniofacial structures is complex and involves multiple cellular and molecular interactions. We report a case of congenital camptodactyly in a female who subsequently developed chronic tinnitus and temporomandibular joint dysfunction. This report describes the clinicoradiographic...

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Autores principales: Aponte, Christina A, Hoffman, Adrienne, Moussa, Selvana, Norvell, Nicholas, Khoury, Zaid H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9760590/
https://www.ncbi.nlm.nih.gov/pubmed/36545157
http://dx.doi.org/10.7759/cureus.31658
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author Aponte, Christina A
Hoffman, Adrienne
Moussa, Selvana
Norvell, Nicholas
Khoury, Zaid H
author_facet Aponte, Christina A
Hoffman, Adrienne
Moussa, Selvana
Norvell, Nicholas
Khoury, Zaid H
author_sort Aponte, Christina A
collection PubMed
description The development of craniofacial structures is complex and involves multiple cellular and molecular interactions. We report a case of congenital camptodactyly in a female who subsequently developed chronic tinnitus and temporomandibular joint dysfunction. This report describes the clinicoradiographic features and surgical management of the facial skeletal manifestations, along with postoperative rehabilitation. Furthermore, a concise review of similar literature raises the question of whether this complex of manifestations represents a new entity or a minimal manifestation of a previously characterized syndrome. As such, a possible developmental association between camptodactyly and temporomandibular joint dysfunction is suggested.
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spelling pubmed-97605902022-12-20 Isolated Congenital Camptodactyly and Temporomandibular Joint Articular Disc Displacement Aponte, Christina A Hoffman, Adrienne Moussa, Selvana Norvell, Nicholas Khoury, Zaid H Cureus Anatomy The development of craniofacial structures is complex and involves multiple cellular and molecular interactions. We report a case of congenital camptodactyly in a female who subsequently developed chronic tinnitus and temporomandibular joint dysfunction. This report describes the clinicoradiographic features and surgical management of the facial skeletal manifestations, along with postoperative rehabilitation. Furthermore, a concise review of similar literature raises the question of whether this complex of manifestations represents a new entity or a minimal manifestation of a previously characterized syndrome. As such, a possible developmental association between camptodactyly and temporomandibular joint dysfunction is suggested. Cureus 2022-11-18 /pmc/articles/PMC9760590/ /pubmed/36545157 http://dx.doi.org/10.7759/cureus.31658 Text en Copyright © 2022, Aponte et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Anatomy
Aponte, Christina A
Hoffman, Adrienne
Moussa, Selvana
Norvell, Nicholas
Khoury, Zaid H
Isolated Congenital Camptodactyly and Temporomandibular Joint Articular Disc Displacement
title Isolated Congenital Camptodactyly and Temporomandibular Joint Articular Disc Displacement
title_full Isolated Congenital Camptodactyly and Temporomandibular Joint Articular Disc Displacement
title_fullStr Isolated Congenital Camptodactyly and Temporomandibular Joint Articular Disc Displacement
title_full_unstemmed Isolated Congenital Camptodactyly and Temporomandibular Joint Articular Disc Displacement
title_short Isolated Congenital Camptodactyly and Temporomandibular Joint Articular Disc Displacement
title_sort isolated congenital camptodactyly and temporomandibular joint articular disc displacement
topic Anatomy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9760590/
https://www.ncbi.nlm.nih.gov/pubmed/36545157
http://dx.doi.org/10.7759/cureus.31658
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