Manejo multidisciplinar da displasia cleidocranial - Revisão de literatura com metanálise

Detalhes bibliográficos
Autor(a) principal: Santana, Gabriela Fernandes
Data de Publicação: 2023
Outros Autores: Souza, Myllena Barbosa de, Nunes, Marina Chaves, Vanzo, Ketlin Lara Tosta, Pereira, Yamba Carla Lara
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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spelling 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
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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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