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Genetics of kidney development: pathogenesis of renal anomalies

Congenital anomalies of the kidney and urinary tract (CAKUT) account for more than 50% of abdominal masses found in neonates and involve about 0.5% of all pregnancies. CAKUT has a major role in renal failure, and increasing evidence suggests that certain abnormalities predispose to the development o...

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Autor principal: Hahn, Hyewon
Formato: Texto
Lenguaje:English
Publicado: The Korean Pediatric Society 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3004483/
https://www.ncbi.nlm.nih.gov/pubmed/21189947
http://dx.doi.org/10.3345/kjp.2010.53.7.729
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author Hahn, Hyewon
author_facet Hahn, Hyewon
author_sort Hahn, Hyewon
collection PubMed
description Congenital anomalies of the kidney and urinary tract (CAKUT) account for more than 50% of abdominal masses found in neonates and involve about 0.5% of all pregnancies. CAKUT has a major role in renal failure, and increasing evidence suggests that certain abnormalities predispose to the development of hypertension and cardiovascular disease in adulthood. To understand the pathogenesis of human renal anomalies, understanding the development of kidney is important. Diverse anomalies of the kidney corresponding to defects at a particular stage of development have been documented recently; however, more research is required to understand the molecular networks underlying kidney development, and such an investigation will provide a clue to the therapeutic intervention for CAKUT.
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spelling pubmed-30044832010-12-28 Genetics of kidney development: pathogenesis of renal anomalies Hahn, Hyewon Korean J Pediatr Review Article Congenital anomalies of the kidney and urinary tract (CAKUT) account for more than 50% of abdominal masses found in neonates and involve about 0.5% of all pregnancies. CAKUT has a major role in renal failure, and increasing evidence suggests that certain abnormalities predispose to the development of hypertension and cardiovascular disease in adulthood. To understand the pathogenesis of human renal anomalies, understanding the development of kidney is important. Diverse anomalies of the kidney corresponding to defects at a particular stage of development have been documented recently; however, more research is required to understand the molecular networks underlying kidney development, and such an investigation will provide a clue to the therapeutic intervention for CAKUT. The Korean Pediatric Society 2010-07 2010-07-31 /pmc/articles/PMC3004483/ /pubmed/21189947 http://dx.doi.org/10.3345/kjp.2010.53.7.729 Text en Copyright © 2010 by The Korean Pediatric Society http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Hahn, Hyewon
Genetics of kidney development: pathogenesis of renal anomalies
title Genetics of kidney development: pathogenesis of renal anomalies
title_full Genetics of kidney development: pathogenesis of renal anomalies
title_fullStr Genetics of kidney development: pathogenesis of renal anomalies
title_full_unstemmed Genetics of kidney development: pathogenesis of renal anomalies
title_short Genetics of kidney development: pathogenesis of renal anomalies
title_sort genetics of kidney development: pathogenesis of renal anomalies
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3004483/
https://www.ncbi.nlm.nih.gov/pubmed/21189947
http://dx.doi.org/10.3345/kjp.2010.53.7.729
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