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Non Syndromic Oligodontia: Case Report

Oligodontia is a rare genetic disorder which represents the congenital absence of more than six teeth in primary, permanent or both dentitions. It is usually a part of a syndrome and seldom occurs as an isolated entity. Genes responsible for non syndromic oligodontia are found to be MSX1 and PAX9 ge...

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Detalles Bibliográficos
Autores principales: Tangade, Pradeep, Batra, Manu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research and Publications Office of Jimma University 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3511903/
https://www.ncbi.nlm.nih.gov/pubmed/23209359
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author Tangade, Pradeep
Batra, Manu
author_facet Tangade, Pradeep
Batra, Manu
author_sort Tangade, Pradeep
collection PubMed
description Oligodontia is a rare genetic disorder which represents the congenital absence of more than six teeth in primary, permanent or both dentitions. It is usually a part of a syndrome and seldom occurs as an isolated entity. Genes responsible for non syndromic oligodontia are found to be MSX1 and PAX9 genes. In this case report a 13 year old boy is presented who had absence of all four second permanent molars and permanent mandibular incisors. The maxillary central incisors presented with conical shape. During physical examination, there was no abnormality in either hairs or nails, perspiration was normal and no congenital clefts of lip or palate was seen. Hence in this case, Oligodontia is not associated with any syndrome which is a rare finding.
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spelling pubmed-35119032012-12-03 Non Syndromic Oligodontia: Case Report Tangade, Pradeep Batra, Manu Ethiop J Health Sci Case Report Oligodontia is a rare genetic disorder which represents the congenital absence of more than six teeth in primary, permanent or both dentitions. It is usually a part of a syndrome and seldom occurs as an isolated entity. Genes responsible for non syndromic oligodontia are found to be MSX1 and PAX9 genes. In this case report a 13 year old boy is presented who had absence of all four second permanent molars and permanent mandibular incisors. The maxillary central incisors presented with conical shape. During physical examination, there was no abnormality in either hairs or nails, perspiration was normal and no congenital clefts of lip or palate was seen. Hence in this case, Oligodontia is not associated with any syndrome which is a rare finding. Research and Publications Office of Jimma University 2012-11 /pmc/articles/PMC3511903/ /pubmed/23209359 Text en Copyright © Jimma University, Research & Publications Office 2012
spellingShingle Case Report
Tangade, Pradeep
Batra, Manu
Non Syndromic Oligodontia: Case Report
title Non Syndromic Oligodontia: Case Report
title_full Non Syndromic Oligodontia: Case Report
title_fullStr Non Syndromic Oligodontia: Case Report
title_full_unstemmed Non Syndromic Oligodontia: Case Report
title_short Non Syndromic Oligodontia: Case Report
title_sort non syndromic oligodontia: case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3511903/
https://www.ncbi.nlm.nih.gov/pubmed/23209359
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