Update about the multidisciplinary treatment of cleft lip and palate - doi:10.5020/18061230.2005.p31

Detalhes bibliográficos
Autor(a) principal: Ribeiro, Erlane Marques
Data de Publicação: 2012
Outros Autores: Moreira, Anna Sylvia Carvalho Goulart
Tipo de documento: Artigo
Idioma: por
Título da fonte: Revista Brasileira em Promoção da Saúde
Texto Completo: https://ojs.unifor.br/RBPS/article/view/864
Resumo: Cleft of the lip and palate (CLP) are included among the more common congenital anomalies.Knowing about the importance of the disease, the objective of this study is to inform and to help the health professionals to establish the correct diagnosis and treatment. This review is based on the relevant literature published. The source of data was MEDLINE, LILACS database and textbooks. The key words used for searching were cleft lip and palate. The CLP occurs in approximately 1/600 newborn babies worldwide. The prevalence varies considerably across geographic areas and ethinic groupings. The genetic of CLP is highly complex and include single-gene causes, chromosomal disorders, polygeneic interactions, environmental risks and gene/environmental risks There is a considerable variation in the proportion of cases of CLP with congenital anomalies and syndromes. Ultrasonography has been used to detect CLP prenatally. The patients with CLP need multidisciplinary surgical and non-surgical treatment with pediatrician, geneticist, psychologist, nutritionist, odontologist. The adequate treatment of CLP is important because their impact on speech, hearing, appearance and cognition has a prolonged and adverse influence on health and social integration. The costs incurred from CLP in terms of morbidity, health care, emotional disturbance, social and employment exclusion are considerable for affected individuals, their families and society. Researches may increase in the understanding of the cause of CLP, improve the treatment for it and lead ultimately to its prevention.
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spelling Update about the multidisciplinary treatment of cleft lip and palate - doi:10.5020/18061230.2005.p31Atualização sobre o tratamento multidisciplinar das fissuras labiais e palatinas - doi:10.5020/18061230.2005.p31fissura lábiopalatinafatores de riscoepidemiologiaanormalidadestratamentoCleft of the lip and palate (CLP) are included among the more common congenital anomalies.Knowing about the importance of the disease, the objective of this study is to inform and to help the health professionals to establish the correct diagnosis and treatment. This review is based on the relevant literature published. The source of data was MEDLINE, LILACS database and textbooks. The key words used for searching were cleft lip and palate. The CLP occurs in approximately 1/600 newborn babies worldwide. The prevalence varies considerably across geographic areas and ethinic groupings. The genetic of CLP is highly complex and include single-gene causes, chromosomal disorders, polygeneic interactions, environmental risks and gene/environmental risks There is a considerable variation in the proportion of cases of CLP with congenital anomalies and syndromes. Ultrasonography has been used to detect CLP prenatally. The patients with CLP need multidisciplinary surgical and non-surgical treatment with pediatrician, geneticist, psychologist, nutritionist, odontologist. The adequate treatment of CLP is important because their impact on speech, hearing, appearance and cognition has a prolonged and adverse influence on health and social integration. The costs incurred from CLP in terms of morbidity, health care, emotional disturbance, social and employment exclusion are considerable for affected individuals, their families and society. Researches may increase in the understanding of the cause of CLP, improve the treatment for it and lead ultimately to its prevention.As fissuras labiopalatais (FLP) estão incluídas entre as anomalias congênitas mais comuns. Conhecendo a importância das FLP, o objetivo desse trabalho é informar e ajudar a profissionais de saúde a estabelecer um diagnóstico e tratamento adequado. Essa revisão é baseada em relevante literatura. A fonte de dados foi MEDLINE, LILACS e livrostexto. As palavras chave utilizadas na pesquisa foram fissura de lábio e palato. As FLP ocorrem em aproximadamente 1/600 nascimentos em todo o mundo. A prevalência varia consideravelmente com regiões geográficas e grupos étnicos. A genética das FLP é extremamente complexa e inclue causas monogênicas, doenças cromossômicas, interações poligênicas, riscos ambientais e entre gene e ambiente. Há uma considerável variação na proporção de casos com FLP associados a anomalias congênitas e síndromes. A ultrassonografia tem sido utilizada para detectar FLP no pré-natal. Os pacientes com FLP necessitam de tratamento multidisciplinar cirúrgico e não-cirúrgico com pediatra, geneticista, psicólogo, nutricionista, odontologista. O tratamento das FLP é importante devido ao seu impacto na fala, audição, aparência e cognição tem uma influência prolongada e adversa na saúde e integração social. O custo causado pelas fissuras labiais e palatinas em termos de morbidade, cuidados de saúde, distúrbios emocionais, sociais e exclusão do trabalho são consideráveis para o indivíduo afetado, sua família e a sociedade. As pesquisas podem aumentar a compreensão das causas de fissuras labiais e palatinas, melhoria do tratamento e principalmente na prevenção.Universidade de Fortaleza2012-01-04info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion"Peer-reviewed Article""Avaliado pelos pares""Avaliado pelos pares"application/pdfhttps://ojs.unifor.br/RBPS/article/view/86410.5020/864Brazilian Journal in Health Promotion; Vol. 18 No. 1 (2005); 31-40Revista Brasileña en Promoción de la Salud; Vol. 18 Núm. 1 (2005); 31-40Revista Brasileira em Promoção da Saúde; v. 18 n. 1 (2005); 31-401806-1230reponame:Revista Brasileira em Promoção da Saúdeinstname:Universidade de Fortaleza (Unifor)instacron:UFORporhttps://ojs.unifor.br/RBPS/article/view/864/pdfRibeiro, Erlane MarquesMoreira, Anna Sylvia Carvalho Goulartinfo:eu-repo/semantics/openAccess2012-01-10T12:17:29Zoai:ojs.ojs.unifor.br:article/864Revistahttps://periodicos.unifor.br/RBPS/oai1806-12301806-1222opendoar:2012-01-10T12:17:29Revista Brasileira em Promoção da Saúde - Universidade de Fortaleza (Unifor)false
dc.title.none.fl_str_mv Update about the multidisciplinary treatment of cleft lip and palate - doi:10.5020/18061230.2005.p31
Atualização sobre o tratamento multidisciplinar das fissuras labiais e palatinas - doi:10.5020/18061230.2005.p31
title Update about the multidisciplinary treatment of cleft lip and palate - doi:10.5020/18061230.2005.p31
spellingShingle Update about the multidisciplinary treatment of cleft lip and palate - doi:10.5020/18061230.2005.p31
Ribeiro, Erlane Marques
fissura lábiopalatina
fatores de risco
epidemiologia
anormalidades
tratamento
title_short Update about the multidisciplinary treatment of cleft lip and palate - doi:10.5020/18061230.2005.p31
title_full Update about the multidisciplinary treatment of cleft lip and palate - doi:10.5020/18061230.2005.p31
title_fullStr Update about the multidisciplinary treatment of cleft lip and palate - doi:10.5020/18061230.2005.p31
title_full_unstemmed Update about the multidisciplinary treatment of cleft lip and palate - doi:10.5020/18061230.2005.p31
title_sort Update about the multidisciplinary treatment of cleft lip and palate - doi:10.5020/18061230.2005.p31
author Ribeiro, Erlane Marques
author_facet Ribeiro, Erlane Marques
Moreira, Anna Sylvia Carvalho Goulart
author_role author
author2 Moreira, Anna Sylvia Carvalho Goulart
author2_role author
dc.contributor.author.fl_str_mv Ribeiro, Erlane Marques
Moreira, Anna Sylvia Carvalho Goulart
dc.subject.por.fl_str_mv fissura lábiopalatina
fatores de risco
epidemiologia
anormalidades
tratamento
topic fissura lábiopalatina
fatores de risco
epidemiologia
anormalidades
tratamento
description Cleft of the lip and palate (CLP) are included among the more common congenital anomalies.Knowing about the importance of the disease, the objective of this study is to inform and to help the health professionals to establish the correct diagnosis and treatment. This review is based on the relevant literature published. The source of data was MEDLINE, LILACS database and textbooks. The key words used for searching were cleft lip and palate. The CLP occurs in approximately 1/600 newborn babies worldwide. The prevalence varies considerably across geographic areas and ethinic groupings. The genetic of CLP is highly complex and include single-gene causes, chromosomal disorders, polygeneic interactions, environmental risks and gene/environmental risks There is a considerable variation in the proportion of cases of CLP with congenital anomalies and syndromes. Ultrasonography has been used to detect CLP prenatally. The patients with CLP need multidisciplinary surgical and non-surgical treatment with pediatrician, geneticist, psychologist, nutritionist, odontologist. The adequate treatment of CLP is important because their impact on speech, hearing, appearance and cognition has a prolonged and adverse influence on health and social integration. The costs incurred from CLP in terms of morbidity, health care, emotional disturbance, social and employment exclusion are considerable for affected individuals, their families and society. Researches may increase in the understanding of the cause of CLP, improve the treatment for it and lead ultimately to its prevention.
publishDate 2012
dc.date.none.fl_str_mv 2012-01-04
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
"Peer-reviewed Article"
"Avaliado pelos pares"
"Avaliado pelos pares"
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://ojs.unifor.br/RBPS/article/view/864
10.5020/864
url https://ojs.unifor.br/RBPS/article/view/864
identifier_str_mv 10.5020/864
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv https://ojs.unifor.br/RBPS/article/view/864/pdf
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade de Fortaleza
publisher.none.fl_str_mv Universidade de Fortaleza
dc.source.none.fl_str_mv Brazilian Journal in Health Promotion; Vol. 18 No. 1 (2005); 31-40
Revista Brasileña en Promoción de la Salud; Vol. 18 Núm. 1 (2005); 31-40
Revista Brasileira em Promoção da Saúde; v. 18 n. 1 (2005); 31-40
1806-1230
reponame:Revista Brasileira em Promoção da Saúde
instname:Universidade de Fortaleza (Unifor)
instacron:UFOR
instname_str Universidade de Fortaleza (Unifor)
instacron_str UFOR
institution UFOR
reponame_str Revista Brasileira em Promoção da Saúde
collection Revista Brasileira em Promoção da Saúde
repository.name.fl_str_mv Revista Brasileira em Promoção da Saúde - Universidade de Fortaleza (Unifor)
repository.mail.fl_str_mv
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