Manejo multidisciplinar da displasia cleidocranial - Revisão de literatura com metanálise
Autor(a) principal: | |
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Data de Publicação: | 2023 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | por |
Título da fonte: | Research, Society and Development |
Texto Completo: | https://rsdjournal.org/index.php/rsd/article/view/42505 |
Resumo: | Introduction: The article in question explains a literature review, clearly presenting Cleidocranial Dysplasia (CCD), in a dental and medical view. Above all, indicating its main clinical manifestations and concomitantly with this, we elucidate an approach through general diagnosis and a dental diagnosis. Objectives: It aims to show how early investigation leads to a good prognosis, highlighting pre- and postnatal care as a decisive factor and, therefore, identifying changes in dysplasia in clinical and complementary exams. Methodology: The article is a literature review with a quali-quantitative approach and meta-analysis. The bibliographical survey was carried out in the databases of Google Scholar, PUBMED and Scielo, in English and Portuguese. The selected articles were those that addressed the theme and had been published in the last ten years. Results: A total of fifteen articles were found. These were subjected to a deep analysis and observed if the subject approached matches the one recommended by the study, obeying the exclusion criteria. Final considerations: Prenatal and postnatal care of patients with the syndrome is necessary to have a predictability of possible skeletal, orodental and orofacial manifestations due to the genetic mutation of RUNX2. In the face of these issues, normally the first professional to be sought is the DSS (Doctor of Dental Surgery), due to the delay in the eruption of the permanent dentition, with late diagnosis being the result of a multidisciplinary association of treatment involving psychologists, doctors of dental surgery, physicians, physiotherapists, speech-language pathologist, nursing team and community agent. |
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Manejo multidisciplinar da displasia cleidocranial - Revisão de literatura com metanálise Multidisciplinary management of cleidocranial dysplasia - Literature review with meta-analysisManejo multidisciplinario de la displasia cleidocraneal - Revisión de la literatura con metanálisisDisplasia cleidocranealOdontologiaDisostosis cleidocranealMedicina clínicaInvestigación multidisciplinar.Displasia cleidocranianaOdontologiaDisostose cleidocranianaMedicina clínicaPesquisa multidisciplinar.DentistryCleidocranial dysplasiaClinical medicineInterdisciplinary research. Introduction: The article in question explains a literature review, clearly presenting Cleidocranial Dysplasia (CCD), in a dental and medical view. Above all, indicating its main clinical manifestations and concomitantly with this, we elucidate an approach through general diagnosis and a dental diagnosis. Objectives: It aims to show how early investigation leads to a good prognosis, highlighting pre- and postnatal care as a decisive factor and, therefore, identifying changes in dysplasia in clinical and complementary exams. Methodology: The article is a literature review with a quali-quantitative approach and meta-analysis. The bibliographical survey was carried out in the databases of Google Scholar, PUBMED and Scielo, in English and Portuguese. The selected articles were those that addressed the theme and had been published in the last ten years. Results: A total of fifteen articles were found. These were subjected to a deep analysis and observed if the subject approached matches the one recommended by the study, obeying the exclusion criteria. Final considerations: Prenatal and postnatal care of patients with the syndrome is necessary to have a predictability of possible skeletal, orodental and orofacial manifestations due to the genetic mutation of RUNX2. In the face of these issues, normally the first professional to be sought is the DSS (Doctor of Dental Surgery), due to the delay in the eruption of the permanent dentition, with late diagnosis being the result of a multidisciplinary association of treatment involving psychologists, doctors of dental surgery, physicians, physiotherapists, speech-language pathologist, nursing team and community agent.Introducción: El artículo en cuestión explica una revisión de la literatura, presentando claramente la Displasia Cleidocraneal (DCC) desde un punto de vista médico e dental. Sobre todo indicando su principales manifestaciones clínicas y concomitantemente a ello, elucidamos un abordaje por diagnóstico general y un diagnóstico odontológico. Objetivos: Pretende mostrar cómo la investigación temprana conduce a un buen pronóstico, destacando la atención prenatal y posnatal como un factor decisivo y, por lo tanto, identificando cambios en la displasia en los exámenes clínicos y complementarios. Metodología: El artículo es una revisión de la literatura con un enfoque cuali-cuantitativo y metanálisis. Y se realizó un levantamiento bibliográfico en las bases de datos de Google Scholar, PUBMED y Scielo, en inglés y portugués. Los artículos seleccionados fueron aquellos que abordaban el tema y habían sido publicados en los últimos diez años. Resultados: Se encontraron un total de quince artículos. Éstos fueron sometidos a un análisis profundo y se observó si el tema abordado coincide con el preconizado por el estudio, obedeciendo a los criterios de exclusión. Consideraciones finales: El seguimiento prenatal y posnatal de los pacientes con el síndrome es necesario para tener una predictibilidad de las posibles manifestaciones esqueléticas, orodentales y orofaciales por la mutación genética de RUNX2. Ante estas cuestiones, el primer profesional que se busca suele ser el CD (Odontólogo), debido al retraso en la erupción de la dentición permanente, siendo el diagnóstico tardío el resultado de una asociación multidisciplinar de tratamiento en la que participan psicólogos, odontólogos, médicos, fisioterapeutas, logopedas, personal de enfermería y agentes comunitarios.Introdução: O artigo em questão, explana uma revisão de literatura, apresentando de maneira clara a Displasia Cleidocraniana (DCC), em uma visão odontológica e médica. Sobretudo, indicando suas principais manifestações clínicas e concomitante a isto, elucidamos uma abordagem pelo diagnóstico geral e um diagnóstico odontológico. Objetivos: Visa apresentar o quanto a investigação precoce leva a um bom prognóstico, evidenciando o acompanhamento pré e pós-natal como um fator decisivo e, portanto, identificando as alterações da displasia em exames clínicos e complementares. Metodologia: O artigo é uma revisão de literatura com abordagem quali-quantitativa e metanálise. E foi realizado um levantamento bibliográfico nas bases de dados do Google Acadêmico, PUBMED e Scielo, em língua inglesa e portuguesa. Os artigos selecionados foram aqueles que abordavam a temática e tinham sido publicados nos últimos dez anos. Resultados: Foram encontrados o total de quinze artigos. Esses foram sujeitos a uma análise profunda e observado se o assunto abordado condiz pelo preconizado pelo estudo, obedecendo os critérios de exclusão. Considerações finais: O acompanhamento pré-natal e pós-natal dos pacientes portadores da síndrome faz-se necessário para se ter uma previsibilidade das possíveis manifestações esqueléticas, orodentais e orofaciais devido a mutação genética do RUNX2. Perante essas questões normalmente o primeiro profissional a ser procurado é o CD (Cirurgião-Dentista), devido ao atraso na erupção da dentição permanente, sendo o diagnóstico tardio e resultado de uma associação multidisciplinar do tratamento envolvendo psicólogos, cirurgiões-dentistas, médicos, fisioterapeutas, fonoaudiólogos, equipe de enfermagem e agente comunitário.Research, Society and Development2023-07-14info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://rsdjournal.org/index.php/rsd/article/view/4250510.33448/rsd-v12i7.42505Research, Society and Development; Vol. 12 No. 7; e5912742505Research, Society and Development; Vol. 12 Núm. 7; e5912742505Research, Society and Development; v. 12 n. 7; e59127425052525-3409reponame:Research, Society and Developmentinstname:Universidade Federal de Itajubá (UNIFEI)instacron:UNIFEIporhttps://rsdjournal.org/index.php/rsd/article/view/42505/34354Copyright (c) 2023 Gabriela Fernandes Santana; Myllena Barbosa de Souza; Marina Chaves Nunes; Ketlin Lara Tosta Vanzo; Yamba Carla Lara Pereirahttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessSantana, Gabriela Fernandes Souza, Myllena Barbosa de Nunes, Marina Chaves Vanzo, Ketlin Lara Tosta Pereira, Yamba Carla Lara 2023-08-03T14:15:19Zoai:ojs.pkp.sfu.ca:article/42505Revistahttps://rsdjournal.org/index.php/rsd/indexPUBhttps://rsdjournal.org/index.php/rsd/oairsd.articles@gmail.com2525-34092525-3409opendoar:2023-08-03T14:15:19Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)false |
dc.title.none.fl_str_mv |
Manejo multidisciplinar da displasia cleidocranial - Revisão de literatura com metanálise Multidisciplinary management of cleidocranial dysplasia - Literature review with meta-analysis Manejo multidisciplinario de la displasia cleidocraneal - Revisión de la literatura con metanálisis |
title |
Manejo multidisciplinar da displasia cleidocranial - Revisão de literatura com metanálise |
spellingShingle |
Manejo multidisciplinar da displasia cleidocranial - Revisão de literatura com metanálise Santana, Gabriela Fernandes Displasia cleidocraneal Odontologia Disostosis cleidocraneal Medicina clínica Investigación multidisciplinar. Displasia cleidocraniana Odontologia Disostose cleidocraniana Medicina clínica Pesquisa multidisciplinar. Dentistry Cleidocranial dysplasia Clinical medicine Interdisciplinary research. |
title_short |
Manejo multidisciplinar da displasia cleidocranial - Revisão de literatura com metanálise |
title_full |
Manejo multidisciplinar da displasia cleidocranial - Revisão de literatura com metanálise |
title_fullStr |
Manejo multidisciplinar da displasia cleidocranial - Revisão de literatura com metanálise |
title_full_unstemmed |
Manejo multidisciplinar da displasia cleidocranial - Revisão de literatura com metanálise |
title_sort |
Manejo multidisciplinar da displasia cleidocranial - Revisão de literatura com metanálise |
author |
Santana, Gabriela Fernandes |
author_facet |
Santana, Gabriela Fernandes Souza, Myllena Barbosa de Nunes, Marina Chaves Vanzo, Ketlin Lara Tosta Pereira, Yamba Carla Lara |
author_role |
author |
author2 |
Souza, Myllena Barbosa de Nunes, Marina Chaves Vanzo, Ketlin Lara Tosta Pereira, Yamba Carla Lara |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Santana, Gabriela Fernandes Souza, Myllena Barbosa de Nunes, Marina Chaves Vanzo, Ketlin Lara Tosta Pereira, Yamba Carla Lara |
dc.subject.por.fl_str_mv |
Displasia cleidocraneal Odontologia Disostosis cleidocraneal Medicina clínica Investigación multidisciplinar. Displasia cleidocraniana Odontologia Disostose cleidocraniana Medicina clínica Pesquisa multidisciplinar. Dentistry Cleidocranial dysplasia Clinical medicine Interdisciplinary research. |
topic |
Displasia cleidocraneal Odontologia Disostosis cleidocraneal Medicina clínica Investigación multidisciplinar. Displasia cleidocraniana Odontologia Disostose cleidocraniana Medicina clínica Pesquisa multidisciplinar. Dentistry Cleidocranial dysplasia Clinical medicine Interdisciplinary research. |
description |
Introduction: The article in question explains a literature review, clearly presenting Cleidocranial Dysplasia (CCD), in a dental and medical view. Above all, indicating its main clinical manifestations and concomitantly with this, we elucidate an approach through general diagnosis and a dental diagnosis. Objectives: It aims to show how early investigation leads to a good prognosis, highlighting pre- and postnatal care as a decisive factor and, therefore, identifying changes in dysplasia in clinical and complementary exams. Methodology: The article is a literature review with a quali-quantitative approach and meta-analysis. The bibliographical survey was carried out in the databases of Google Scholar, PUBMED and Scielo, in English and Portuguese. The selected articles were those that addressed the theme and had been published in the last ten years. Results: A total of fifteen articles were found. These were subjected to a deep analysis and observed if the subject approached matches the one recommended by the study, obeying the exclusion criteria. Final considerations: Prenatal and postnatal care of patients with the syndrome is necessary to have a predictability of possible skeletal, orodental and orofacial manifestations due to the genetic mutation of RUNX2. In the face of these issues, normally the first professional to be sought is the DSS (Doctor of Dental Surgery), due to the delay in the eruption of the permanent dentition, with late diagnosis being the result of a multidisciplinary association of treatment involving psychologists, doctors of dental surgery, physicians, physiotherapists, speech-language pathologist, nursing team and community agent. |
publishDate |
2023 |
dc.date.none.fl_str_mv |
2023-07-14 |
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/42505 10.33448/rsd-v12i7.42505 |
url |
https://rsdjournal.org/index.php/rsd/article/view/42505 |
identifier_str_mv |
10.33448/rsd-v12i7.42505 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.none.fl_str_mv |
https://rsdjournal.org/index.php/rsd/article/view/42505/34354 |
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. 12 No. 7; e5912742505 Research, Society and Development; Vol. 12 Núm. 7; e5912742505 Research, Society and Development; v. 12 n. 7; e5912742505 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 |
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1797052627821789184 |