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Congenital Kidney and Urinary Tract Anomalies: a Review for Nephrologists

dc.contributor.authorVieira, M
dc.contributor.authorFerreira, A
dc.contributor.authorNolasco, F
dc.date.accessioned2021-09-08T11:06:28Z
dc.date.available2021-09-08T11:06:28Z
dc.date.issued2018
dc.description.abstractKidney 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 neph‑ rologist 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.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationPort J Nephrol Hypert 2018;32(4):385-391pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.17/3844
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherSociedade Portuguesa de Nefrologia e Hipertensãopt_PT
dc.subjectHCC NEFpt_PT
dc.subjectDysplasiapt_PT
dc.subjectCiliopathiespt_PT
dc.subjectPosterior Urethral Valvespt_PT
dc.subjectCongenital Anomaliespt_PT
dc.titleCongenital Kidney and Urinary Tract Anomalies: a Review for Nephrologistspt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage391pt_PT
oaire.citation.startPage385pt_PT
oaire.citation.titlePortuguese Journal of Nephrology and Hypertensionpt_PT
oaire.citation.volume32pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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