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Solitary median maxillary central incisor syndrome: A rare entity

Solitary median maxillary central incisor (SMMCI) syndrome is a complex disorder and a rare dental anomaly, which is estimated to occur in approximately 1:50,000 live births. It is a unique developmental abnormality which involves the central incisor tooth germs, occurring with or without systemic i...

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Detalles Bibliográficos
Autores principales: Negi, Anurag, Negi, Amita, Mohanan, Megha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7802849/
https://www.ncbi.nlm.nih.gov/pubmed/33456262
http://dx.doi.org/10.4103/jomfp.JOMFP_183_19
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author Negi, Anurag
Negi, Amita
Mohanan, Megha
author_facet Negi, Anurag
Negi, Amita
Mohanan, Megha
author_sort Negi, Anurag
collection PubMed
description Solitary median maxillary central incisor (SMMCI) syndrome is a complex disorder and a rare dental anomaly, which is estimated to occur in approximately 1:50,000 live births. It is a unique developmental abnormality which involves the central incisor tooth germs, occurring with or without systemic involvement; hence, its early diagnosis is of great importance. The objective of this study was to discuss a case of SMMCI syndrome and various dental treatment alternatives available in management of such cases. Due to the possible association of this syndrome with other developmental problems, an early diagnosis and management becomes important. Moreover, when it is associated with other developmental malformation and defects, the management becomes multidisciplinary.
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spelling pubmed-78028492021-01-15 Solitary median maxillary central incisor syndrome: A rare entity Negi, Anurag Negi, Amita Mohanan, Megha J Oral Maxillofac Pathol Case Report Solitary median maxillary central incisor (SMMCI) syndrome is a complex disorder and a rare dental anomaly, which is estimated to occur in approximately 1:50,000 live births. It is a unique developmental abnormality which involves the central incisor tooth germs, occurring with or without systemic involvement; hence, its early diagnosis is of great importance. The objective of this study was to discuss a case of SMMCI syndrome and various dental treatment alternatives available in management of such cases. Due to the possible association of this syndrome with other developmental problems, an early diagnosis and management becomes important. Moreover, when it is associated with other developmental malformation and defects, the management becomes multidisciplinary. Wolters Kluwer - Medknow 2020 2020-09-09 /pmc/articles/PMC7802849/ /pubmed/33456262 http://dx.doi.org/10.4103/jomfp.JOMFP_183_19 Text en Copyright: © 2020 Journal of Oral and Maxillofacial Pathology http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Negi, Anurag
Negi, Amita
Mohanan, Megha
Solitary median maxillary central incisor syndrome: A rare entity
title Solitary median maxillary central incisor syndrome: A rare entity
title_full Solitary median maxillary central incisor syndrome: A rare entity
title_fullStr Solitary median maxillary central incisor syndrome: A rare entity
title_full_unstemmed Solitary median maxillary central incisor syndrome: A rare entity
title_short Solitary median maxillary central incisor syndrome: A rare entity
title_sort solitary median maxillary central incisor syndrome: a rare entity
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7802849/
https://www.ncbi.nlm.nih.gov/pubmed/33456262
http://dx.doi.org/10.4103/jomfp.JOMFP_183_19
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