Dental anomalies of a child with incontinentia pigmenti: Case report

Detalhes bibliográficos
Autor(a) principal: Regis , Wanessa Fernandes Matias
Data de Publicação: 2021
Outros Autores: Neves , Beatriz Gonçalves, Lima, Ramille Araújo, Rocha , Francisco Ruliglésio, Rodrigues , Lidiany Karla Azevedo
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Research, Society and Development
Texto Completo: https://rsdjournal.org/index.php/rsd/article/view/17482
Resumo: Incontinentia Pigmenti is a rare multi-system dominant genetic disorder caused by a mutation of the IKBKG/NEMO gene, localized on the X-chromosome, locus Xq28, characterized by dermatological, ocular, neurological, and dental alterations. This case report shows Incontinentia Pigmenti dental findings and emphasizes the importance of the dentist's knowledge about these anomalies so that the patient can be regularly monitored throughout the development of the dentition. Keywords: Child, Incontinentia Pigmenti, Tooth Abnormalities.
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spelling Dental anomalies of a child with incontinentia pigmenti: Case reportAnomalías dentales en niño con incontinencia pigmentaria: Reporte de casoAnomalias dentárias de uma criança com incontinência pigmentar: Relato de casoCriançaIncontinentia PigmentiAnormalidades dentárias.ChildIncontinentia PigmentiTooth abnormalities.NiñoIncontinentia PigmentiAnormalidades dentales.Incontinentia Pigmenti is a rare multi-system dominant genetic disorder caused by a mutation of the IKBKG/NEMO gene, localized on the X-chromosome, locus Xq28, characterized by dermatological, ocular, neurological, and dental alterations. This case report shows Incontinentia Pigmenti dental findings and emphasizes the importance of the dentist's knowledge about these anomalies so that the patient can be regularly monitored throughout the development of the dentition. Keywords: Child, Incontinentia Pigmenti, Tooth Abnormalities.Incontinentia Pigmenti es un trastorno genético dominante multisistémico poco común causado por una mutación del gen IKBKG / NEMO, localizado en el cromosoma X, locus Xq28, caracterizado por alteraciones dermatológicas, oculares, neurológicas y dentales. Este informe de caso muestra los hallazgos dentales de Incontinentia Pigmenti y enfatiza la importancia del conocimiento del dentista sobre estas anomalías para que el paciente pueda ser monitoreado regularmente durante el desarrollo de la dentición.Incontinentia Pigmenti é uma doença genética multissistêmica dominante rara, causada por uma mutação do gene IKBKG / NEMO, localizada no cromossomo X, locus Xq28, caracterizada por alterações dermatológicas, oculares, neurológicas e dentais. Este relato de caso mostra os achados odontológicos da Incontinentia Pigmenti e enfatiza a importância do conhecimento do dentista sobre essas anomalias para que o paciente possa ser monitorado regularmente durante todo o desenvolvimento da dentição.Research, Society and Development2021-08-03info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://rsdjournal.org/index.php/rsd/article/view/1748210.33448/rsd-v10i9.17482Research, Society and Development; Vol. 10 No. 9; e50310917482Research, Society and Development; Vol. 10 Núm. 9; e50310917482Research, Society and Development; v. 10 n. 9; e503109174822525-3409reponame:Research, Society and Developmentinstname:Universidade Federal de Itajubá (UNIFEI)instacron:UNIFEIenghttps://rsdjournal.org/index.php/rsd/article/view/17482/16510Copyright (c) 2021 Wanessa Fernandes Matias Regis ; Beatriz Gonçalves Neves ; Ramille Araújo Lima; Francisco Ruliglésio Rocha ; Lidiany Karla Azevedo Rodrigues https://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessRegis , Wanessa Fernandes MatiasNeves , Beatriz Gonçalves Lima, Ramille Araújo Rocha , Francisco Ruliglésio Rodrigues , Lidiany Karla Azevedo 2021-09-12T14:28:06Zoai:ojs.pkp.sfu.ca:article/17482Revistahttps://rsdjournal.org/index.php/rsd/indexPUBhttps://rsdjournal.org/index.php/rsd/oairsd.articles@gmail.com2525-34092525-3409opendoar:2024-01-17T09:37:48.459447Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)false
dc.title.none.fl_str_mv Dental anomalies of a child with incontinentia pigmenti: Case report
Anomalías dentales en niño con incontinencia pigmentaria: Reporte de caso
Anomalias dentárias de uma criança com incontinência pigmentar: Relato de caso
title Dental anomalies of a child with incontinentia pigmenti: Case report
spellingShingle Dental anomalies of a child with incontinentia pigmenti: Case report
Regis , Wanessa Fernandes Matias
Criança
Incontinentia Pigmenti
Anormalidades dentárias.
Child
Incontinentia Pigmenti
Tooth abnormalities.
Niño
Incontinentia Pigmenti
Anormalidades dentales.
title_short Dental anomalies of a child with incontinentia pigmenti: Case report
title_full Dental anomalies of a child with incontinentia pigmenti: Case report
title_fullStr Dental anomalies of a child with incontinentia pigmenti: Case report
title_full_unstemmed Dental anomalies of a child with incontinentia pigmenti: Case report
title_sort Dental anomalies of a child with incontinentia pigmenti: Case report
author Regis , Wanessa Fernandes Matias
author_facet Regis , Wanessa Fernandes Matias
Neves , Beatriz Gonçalves
Lima, Ramille Araújo
Rocha , Francisco Ruliglésio
Rodrigues , Lidiany Karla Azevedo
author_role author
author2 Neves , Beatriz Gonçalves
Lima, Ramille Araújo
Rocha , Francisco Ruliglésio
Rodrigues , Lidiany Karla Azevedo
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Regis , Wanessa Fernandes Matias
Neves , Beatriz Gonçalves
Lima, Ramille Araújo
Rocha , Francisco Ruliglésio
Rodrigues , Lidiany Karla Azevedo
dc.subject.por.fl_str_mv Criança
Incontinentia Pigmenti
Anormalidades dentárias.
Child
Incontinentia Pigmenti
Tooth abnormalities.
Niño
Incontinentia Pigmenti
Anormalidades dentales.
topic Criança
Incontinentia Pigmenti
Anormalidades dentárias.
Child
Incontinentia Pigmenti
Tooth abnormalities.
Niño
Incontinentia Pigmenti
Anormalidades dentales.
description Incontinentia Pigmenti is a rare multi-system dominant genetic disorder caused by a mutation of the IKBKG/NEMO gene, localized on the X-chromosome, locus Xq28, characterized by dermatological, ocular, neurological, and dental alterations. This case report shows Incontinentia Pigmenti dental findings and emphasizes the importance of the dentist's knowledge about these anomalies so that the patient can be regularly monitored throughout the development of the dentition. Keywords: Child, Incontinentia Pigmenti, Tooth Abnormalities.
publishDate 2021
dc.date.none.fl_str_mv 2021-08-03
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://rsdjournal.org/index.php/rsd/article/view/17482
10.33448/rsd-v10i9.17482
url https://rsdjournal.org/index.php/rsd/article/view/17482
identifier_str_mv 10.33448/rsd-v10i9.17482
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://rsdjournal.org/index.php/rsd/article/view/17482/16510
dc.rights.driver.fl_str_mv https://creativecommons.org/licenses/by/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Research, Society and Development
publisher.none.fl_str_mv Research, Society and Development
dc.source.none.fl_str_mv Research, Society and Development; Vol. 10 No. 9; e50310917482
Research, Society and Development; Vol. 10 Núm. 9; e50310917482
Research, Society and Development; v. 10 n. 9; e50310917482
2525-3409
reponame:Research, Society and Development
instname:Universidade Federal de Itajubá (UNIFEI)
instacron:UNIFEI
instname_str Universidade Federal de Itajubá (UNIFEI)
instacron_str UNIFEI
institution UNIFEI
reponame_str Research, Society and Development
collection Research, Society and Development
repository.name.fl_str_mv Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)
repository.mail.fl_str_mv rsd.articles@gmail.com
_version_ 1797052682467278848

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