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Dental and Craniofacial Manifestation of Axenfeld-Rieger Syndrome: A Case Report

Axenfeld-Rieger syndrome (ARS) is an autosomal dominant syndrome with a prevalence estimated at 1:50000 to 1:100000 in newborns. It is mainly characterized by ocular, craniofacial, and dental abnormalities. From the pediatric dentist's point of view, early diagnosis of the syndrome from the ocu...

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Autores principales: Badnaware, Sheetal, Srivastava, Vinay Kumar, Chandel, Meenakshi, Gupta, Pooja, Fulzele, Punit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9339346/
https://www.ncbi.nlm.nih.gov/pubmed/35923678
http://dx.doi.org/10.7759/cureus.26442
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author Badnaware, Sheetal
Srivastava, Vinay Kumar
Chandel, Meenakshi
Gupta, Pooja
Fulzele, Punit
author_facet Badnaware, Sheetal
Srivastava, Vinay Kumar
Chandel, Meenakshi
Gupta, Pooja
Fulzele, Punit
author_sort Badnaware, Sheetal
collection PubMed
description Axenfeld-Rieger syndrome (ARS) is an autosomal dominant syndrome with a prevalence estimated at 1:50000 to 1:100000 in newborns. It is mainly characterized by ocular, craniofacial, and dental abnormalities. From the pediatric dentist's point of view, early diagnosis of the syndrome from the ocular, craniofacial, and dental manifestation can prevent further abnormalities and ocular complications such as glaucoma. This case report presents a brief description of ARS with the characteristics of craniofacial and dental findings.
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spelling pubmed-93393462022-08-02 Dental and Craniofacial Manifestation of Axenfeld-Rieger Syndrome: A Case Report Badnaware, Sheetal Srivastava, Vinay Kumar Chandel, Meenakshi Gupta, Pooja Fulzele, Punit Cureus Genetics Axenfeld-Rieger syndrome (ARS) is an autosomal dominant syndrome with a prevalence estimated at 1:50000 to 1:100000 in newborns. It is mainly characterized by ocular, craniofacial, and dental abnormalities. From the pediatric dentist's point of view, early diagnosis of the syndrome from the ocular, craniofacial, and dental manifestation can prevent further abnormalities and ocular complications such as glaucoma. This case report presents a brief description of ARS with the characteristics of craniofacial and dental findings. Cureus 2022-06-29 /pmc/articles/PMC9339346/ /pubmed/35923678 http://dx.doi.org/10.7759/cureus.26442 Text en Copyright © 2022, Badnaware 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 Genetics
Badnaware, Sheetal
Srivastava, Vinay Kumar
Chandel, Meenakshi
Gupta, Pooja
Fulzele, Punit
Dental and Craniofacial Manifestation of Axenfeld-Rieger Syndrome: A Case Report
title Dental and Craniofacial Manifestation of Axenfeld-Rieger Syndrome: A Case Report
title_full Dental and Craniofacial Manifestation of Axenfeld-Rieger Syndrome: A Case Report
title_fullStr Dental and Craniofacial Manifestation of Axenfeld-Rieger Syndrome: A Case Report
title_full_unstemmed Dental and Craniofacial Manifestation of Axenfeld-Rieger Syndrome: A Case Report
title_short Dental and Craniofacial Manifestation of Axenfeld-Rieger Syndrome: A Case Report
title_sort dental and craniofacial manifestation of axenfeld-rieger syndrome: a case report
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9339346/
https://www.ncbi.nlm.nih.gov/pubmed/35923678
http://dx.doi.org/10.7759/cureus.26442
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