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Non-syndromic multiple supernumerary teeth in a family unit with a normal karyotype: case report

Introduction. Hyperdontia is an odontostomatologic anomaly characterized by an excess in tooth number. It seems to occur more often in patients with hereditary factors concerning this anomaly: this case represents a rare form of hyperdontia, with bilateral multiple supernumerary teeth, with evident...

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Autores principales: Inchingolo, Francesco, Tatullo, Marco, Abenavoli, Fabio M., Marrelli, Massimo, Inchingolo, Alessio D., Gentile, Mattia, Inchingolo, Angelo M., Dipalma, Gianna
Formato: Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2974166/
https://www.ncbi.nlm.nih.gov/pubmed/21060725
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author Inchingolo, Francesco
Tatullo, Marco
Abenavoli, Fabio M.
Marrelli, Massimo
Inchingolo, Alessio D.
Gentile, Mattia
Inchingolo, Angelo M.
Dipalma, Gianna
author_facet Inchingolo, Francesco
Tatullo, Marco
Abenavoli, Fabio M.
Marrelli, Massimo
Inchingolo, Alessio D.
Gentile, Mattia
Inchingolo, Angelo M.
Dipalma, Gianna
author_sort Inchingolo, Francesco
collection PubMed
description Introduction. Hyperdontia is an odontostomatologic anomaly characterized by an excess in tooth number. It seems to occur more often in patients with hereditary factors concerning this anomaly: this case represents a rare form of hyperdontia, with bilateral multiple supernumerary teeth, with evident penetrance of the phenotype in the family unit engaged in the present study. The karyotype determination excludes a pathogenesis on chromosomal basis. Case report. A 30 years old patient came to our observation with five impacted teeth (1.8, 2.8, 3.8, 4.7 and 4.8), as well as with the presence of an impacted supernumerary tooth (distomolar 4.9). The patient was suggested to allow us to perform a radiologic screening to his two sisters aged 17 and 13 years. The X-ray photography showed that the elder sister had nine impacted teeth; these were 1.8 - 1.9 - 2.8 - 2.9 - 2.10 - 3.8 - 3.9 - 4.8 - 4.9; while the youngest sister had four impacted teeth, that is 1.8 - 1.9 - 2.8 - 2.9. Conclusions. The value of the present case report can be used as a paradigm for the assessment of the hereditary factors predisposing the onset of hyperdontia, and for the consequent management by oral surgeon of family units in which the odontostomatologic anomaly was detected without any syndromic forms.
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spelling pubmed-29741662010-11-08 Non-syndromic multiple supernumerary teeth in a family unit with a normal karyotype: case report Inchingolo, Francesco Tatullo, Marco Abenavoli, Fabio M. Marrelli, Massimo Inchingolo, Alessio D. Gentile, Mattia Inchingolo, Angelo M. Dipalma, Gianna Int J Med Sci Case Report Introduction. Hyperdontia is an odontostomatologic anomaly characterized by an excess in tooth number. It seems to occur more often in patients with hereditary factors concerning this anomaly: this case represents a rare form of hyperdontia, with bilateral multiple supernumerary teeth, with evident penetrance of the phenotype in the family unit engaged in the present study. The karyotype determination excludes a pathogenesis on chromosomal basis. Case report. A 30 years old patient came to our observation with five impacted teeth (1.8, 2.8, 3.8, 4.7 and 4.8), as well as with the presence of an impacted supernumerary tooth (distomolar 4.9). The patient was suggested to allow us to perform a radiologic screening to his two sisters aged 17 and 13 years. The X-ray photography showed that the elder sister had nine impacted teeth; these were 1.8 - 1.9 - 2.8 - 2.9 - 2.10 - 3.8 - 3.9 - 4.8 - 4.9; while the youngest sister had four impacted teeth, that is 1.8 - 1.9 - 2.8 - 2.9. Conclusions. The value of the present case report can be used as a paradigm for the assessment of the hereditary factors predisposing the onset of hyperdontia, and for the consequent management by oral surgeon of family units in which the odontostomatologic anomaly was detected without any syndromic forms. Ivyspring International Publisher 2010-11-05 /pmc/articles/PMC2974166/ /pubmed/21060725 Text en © Ivyspring International Publisher. This is an open-access article distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited.
spellingShingle Case Report
Inchingolo, Francesco
Tatullo, Marco
Abenavoli, Fabio M.
Marrelli, Massimo
Inchingolo, Alessio D.
Gentile, Mattia
Inchingolo, Angelo M.
Dipalma, Gianna
Non-syndromic multiple supernumerary teeth in a family unit with a normal karyotype: case report
title Non-syndromic multiple supernumerary teeth in a family unit with a normal karyotype: case report
title_full Non-syndromic multiple supernumerary teeth in a family unit with a normal karyotype: case report
title_fullStr Non-syndromic multiple supernumerary teeth in a family unit with a normal karyotype: case report
title_full_unstemmed Non-syndromic multiple supernumerary teeth in a family unit with a normal karyotype: case report
title_short Non-syndromic multiple supernumerary teeth in a family unit with a normal karyotype: case report
title_sort non-syndromic multiple supernumerary teeth in a family unit with a normal karyotype: case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2974166/
https://www.ncbi.nlm.nih.gov/pubmed/21060725
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