Congenital kidney and urinary tract anomalies: a review for nephrologists

Detalhes bibliográficos
Autor(a) principal: Vieira,Marina
Data de Publicação: 2018
Outros Autores: Ferreira,Aníbal, Nolasco,Fernando
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692018000400006
Resumo: Kidney and urinary tract development disorder are two of the most prevalent congenital malformations and the main cause of chronic kidney disease in pediatric age patients. As such, it is very important that the nephrologist understands these pathologies to improve transition and ensure a good continuity between pediatric and adult nephrological care. The purpose of this article is to present a brief review of congenital anomalies of the kidney and urinary tract (CAKUT). Kidney malformations are classified according to macroscopic and microscopic anatomic features, and are the result of the following abnormal renal developmental processes: malformations of the renal parenchyma, abnormalities of the embryonic migration of the kidneys and abnormalities of the developing urinary collecting system.
id RCAP_33e1648e6402eec42787fe4669632834
oai_identifier_str oai:scielo:S0872-01692018000400006
network_acronym_str RCAP
network_name_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository_id_str 7160
spelling Congenital kidney and urinary tract anomalies: a review for nephrologistscongenital anomalies of the kidneys and urinary tractdysplasiaciliopathiesposterior urethral valvesvesicoureteral refluxKidney and urinary tract development disorder are two of the most prevalent congenital malformations and the main cause of chronic kidney disease in pediatric age patients. As such, it is very important that the nephrologist understands these pathologies to improve transition and ensure a good continuity between pediatric and adult nephrological care. The purpose of this article is to present a brief review of congenital anomalies of the kidney and urinary tract (CAKUT). Kidney malformations are classified according to macroscopic and microscopic anatomic features, and are the result of the following abnormal renal developmental processes: malformations of the renal parenchyma, abnormalities of the embryonic migration of the kidneys and abnormalities of the developing urinary collecting system.Sociedade Portuguesa de Nefrologia2018-12-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articletext/htmlhttp://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692018000400006Portuguese Journal of Nephrology & Hypertension v.32 n.4 2018reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPenghttp://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692018000400006Vieira,MarinaFerreira,AníbalNolasco,Fernandoinfo:eu-repo/semantics/openAccess2024-02-06T17:05:00Zoai:scielo:S0872-01692018000400006Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T02:19:01.428624Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Congenital kidney and urinary tract anomalies: a review for nephrologists
title Congenital kidney and urinary tract anomalies: a review for nephrologists
spellingShingle Congenital kidney and urinary tract anomalies: a review for nephrologists
Vieira,Marina
congenital anomalies of the kidneys and urinary tract
dysplasia
ciliopathies
posterior urethral valves
vesicoureteral reflux
title_short Congenital kidney and urinary tract anomalies: a review for nephrologists
title_full Congenital kidney and urinary tract anomalies: a review for nephrologists
title_fullStr Congenital kidney and urinary tract anomalies: a review for nephrologists
title_full_unstemmed Congenital kidney and urinary tract anomalies: a review for nephrologists
title_sort Congenital kidney and urinary tract anomalies: a review for nephrologists
author Vieira,Marina
author_facet Vieira,Marina
Ferreira,Aníbal
Nolasco,Fernando
author_role author
author2 Ferreira,Aníbal
Nolasco,Fernando
author2_role author
author
dc.contributor.author.fl_str_mv Vieira,Marina
Ferreira,Aníbal
Nolasco,Fernando
dc.subject.por.fl_str_mv congenital anomalies of the kidneys and urinary tract
dysplasia
ciliopathies
posterior urethral valves
vesicoureteral reflux
topic congenital anomalies of the kidneys and urinary tract
dysplasia
ciliopathies
posterior urethral valves
vesicoureteral reflux
description Kidney and urinary tract development disorder are two of the most prevalent congenital malformations and the main cause of chronic kidney disease in pediatric age patients. As such, it is very important that the nephrologist understands these pathologies to improve transition and ensure a good continuity between pediatric and adult nephrological care. The purpose of this article is to present a brief review of congenital anomalies of the kidney and urinary tract (CAKUT). Kidney malformations are classified according to macroscopic and microscopic anatomic features, and are the result of the following abnormal renal developmental processes: malformations of the renal parenchyma, abnormalities of the embryonic migration of the kidneys and abnormalities of the developing urinary collecting system.
publishDate 2018
dc.date.none.fl_str_mv 2018-12-01
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692018000400006
url http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692018000400006
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692018000400006
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Portuguesa de Nefrologia
publisher.none.fl_str_mv Sociedade Portuguesa de Nefrologia
dc.source.none.fl_str_mv Portuguese Journal of Nephrology & Hypertension v.32 n.4 2018
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
repository.mail.fl_str_mv
_version_ 1799137280139460608

Registros relacionados