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Solitary Median Maxillary Central Incisor in Hartsfield Syndrome: A Case Report
Hartsfield syndrome is a rare and unique clinical combination of ectrodactyly and holoprosencephaly (HPE) with or without cleft lip and palate, as well as various additional characteristics. Although several genes responsible for HPE and ectrodactyly have been identified, the genetic origin of Harts...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Jaypee Brothers Medical Publishers
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10067985/ https://www.ncbi.nlm.nih.gov/pubmed/37020764 http://dx.doi.org/10.5005/jp-journals-10005-2498 |
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author | Reis, Patricia MP Faber, Jorge Rosa, Jéssica SO Bueno, Mike Barriviera, Maurício Lia, Érica N |
author_facet | Reis, Patricia MP Faber, Jorge Rosa, Jéssica SO Bueno, Mike Barriviera, Maurício Lia, Érica N |
author_sort | Reis, Patricia MP |
collection | PubMed |
description | Hartsfield syndrome is a rare and unique clinical combination of ectrodactyly and holoprosencephaly (HPE) with or without cleft lip and palate, as well as various additional characteristics. Although several genes responsible for HPE and ectrodactyly have been identified, the genetic origin of Hartsfield syndrome remains unknown, as there are few reports in the literature. The objective of this case report is to present dentofacial abnormalities in an 11-year-old boy with Hartsfield syndrome, who presented mental retardation, hearing loss, bilateral hand and foot ectrodactyly, HPE, and solitary median maxillary central incisor (SMMCI) besides 12 dental ageneses. HOW TO CITE THIS ARTICLE: P Reis PM, Faber J, O Rosa JS, et al. Solitary Median Maxillary Central Incisor in Hartsfield Syndrome: A Case Report. Int J Clin Pediatr Dent 2023;16(1):147-152. |
format | Online Article Text |
id | pubmed-10067985 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Jaypee Brothers Medical Publishers |
record_format | MEDLINE/PubMed |
spelling | pubmed-100679852023-04-04 Solitary Median Maxillary Central Incisor in Hartsfield Syndrome: A Case Report Reis, Patricia MP Faber, Jorge Rosa, Jéssica SO Bueno, Mike Barriviera, Maurício Lia, Érica N Int J Clin Pediatr Dent Case Report Hartsfield syndrome is a rare and unique clinical combination of ectrodactyly and holoprosencephaly (HPE) with or without cleft lip and palate, as well as various additional characteristics. Although several genes responsible for HPE and ectrodactyly have been identified, the genetic origin of Hartsfield syndrome remains unknown, as there are few reports in the literature. The objective of this case report is to present dentofacial abnormalities in an 11-year-old boy with Hartsfield syndrome, who presented mental retardation, hearing loss, bilateral hand and foot ectrodactyly, HPE, and solitary median maxillary central incisor (SMMCI) besides 12 dental ageneses. HOW TO CITE THIS ARTICLE: P Reis PM, Faber J, O Rosa JS, et al. Solitary Median Maxillary Central Incisor in Hartsfield Syndrome: A Case Report. Int J Clin Pediatr Dent 2023;16(1):147-152. Jaypee Brothers Medical Publishers 2023 /pmc/articles/PMC10067985/ /pubmed/37020764 http://dx.doi.org/10.5005/jp-journals-10005-2498 Text en Copyright © 2023; The Author(s). https://creativecommons.org/licenses/by-nc/4.0/© The Author(s). 2023 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted use, distribution, and non-commercial reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Reis, Patricia MP Faber, Jorge Rosa, Jéssica SO Bueno, Mike Barriviera, Maurício Lia, Érica N Solitary Median Maxillary Central Incisor in Hartsfield Syndrome: A Case Report |
title | Solitary Median Maxillary Central Incisor in Hartsfield Syndrome: A Case Report |
title_full | Solitary Median Maxillary Central Incisor in Hartsfield Syndrome: A Case Report |
title_fullStr | Solitary Median Maxillary Central Incisor in Hartsfield Syndrome: A Case Report |
title_full_unstemmed | Solitary Median Maxillary Central Incisor in Hartsfield Syndrome: A Case Report |
title_short | Solitary Median Maxillary Central Incisor in Hartsfield Syndrome: A Case Report |
title_sort | solitary median maxillary central incisor in hartsfield syndrome: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10067985/ https://www.ncbi.nlm.nih.gov/pubmed/37020764 http://dx.doi.org/10.5005/jp-journals-10005-2498 |
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