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Jacob’s Disease: Case Series, Extensive Literature Review and Classification Proposal

Jacob’s disease is a rare entity consisting of the formation of a pseudojoint between an abnormal coronoid process of the mandible and the inner surface of the zygomatic bone. First described by Jacob in 1899, its diagnosis and definition have never been entirely univocal. In this paper, we present...

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Autores principales: Raccampo, Luca, Panozzo, Giorgio, Tel, Alessandro, Di Cosola, Michele, Colapinto, Gianluca, Trevisiol, Lorenzo, D’agostino, Antonio, Sembronio, Salvatore, Robiony, Massimo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9917974/
https://www.ncbi.nlm.nih.gov/pubmed/36769586
http://dx.doi.org/10.3390/jcm12030938
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author Raccampo, Luca
Panozzo, Giorgio
Tel, Alessandro
Di Cosola, Michele
Colapinto, Gianluca
Trevisiol, Lorenzo
D’agostino, Antonio
Sembronio, Salvatore
Robiony, Massimo
author_facet Raccampo, Luca
Panozzo, Giorgio
Tel, Alessandro
Di Cosola, Michele
Colapinto, Gianluca
Trevisiol, Lorenzo
D’agostino, Antonio
Sembronio, Salvatore
Robiony, Massimo
author_sort Raccampo, Luca
collection PubMed
description Jacob’s disease is a rare entity consisting of the formation of a pseudojoint between an abnormal coronoid process of the mandible and the inner surface of the zygomatic bone. First described by Jacob in 1899, its diagnosis and definition have never been entirely univocal. In this paper, we present three emblematic cases and an extensive review of the literature on Jacob’s disease. Given the variability observed in the presentation of the disease, we have developed a proposal for the classification, here reported.
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spelling pubmed-99179742023-02-11 Jacob’s Disease: Case Series, Extensive Literature Review and Classification Proposal Raccampo, Luca Panozzo, Giorgio Tel, Alessandro Di Cosola, Michele Colapinto, Gianluca Trevisiol, Lorenzo D’agostino, Antonio Sembronio, Salvatore Robiony, Massimo J Clin Med Case Report Jacob’s disease is a rare entity consisting of the formation of a pseudojoint between an abnormal coronoid process of the mandible and the inner surface of the zygomatic bone. First described by Jacob in 1899, its diagnosis and definition have never been entirely univocal. In this paper, we present three emblematic cases and an extensive review of the literature on Jacob’s disease. Given the variability observed in the presentation of the disease, we have developed a proposal for the classification, here reported. MDPI 2023-01-25 /pmc/articles/PMC9917974/ /pubmed/36769586 http://dx.doi.org/10.3390/jcm12030938 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 Case Report
Raccampo, Luca
Panozzo, Giorgio
Tel, Alessandro
Di Cosola, Michele
Colapinto, Gianluca
Trevisiol, Lorenzo
D’agostino, Antonio
Sembronio, Salvatore
Robiony, Massimo
Jacob’s Disease: Case Series, Extensive Literature Review and Classification Proposal
title Jacob’s Disease: Case Series, Extensive Literature Review and Classification Proposal
title_full Jacob’s Disease: Case Series, Extensive Literature Review and Classification Proposal
title_fullStr Jacob’s Disease: Case Series, Extensive Literature Review and Classification Proposal
title_full_unstemmed Jacob’s Disease: Case Series, Extensive Literature Review and Classification Proposal
title_short Jacob’s Disease: Case Series, Extensive Literature Review and Classification Proposal
title_sort jacob’s disease: case series, extensive literature review and classification proposal
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9917974/
https://www.ncbi.nlm.nih.gov/pubmed/36769586
http://dx.doi.org/10.3390/jcm12030938
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