Severe Prenatal Renal Anomalies Associated with Mutations in HNF1B or PAX2 Genes

BACKGROUND AND OBJECTIVES: Congenital anomalies of the kidney and urinary tract (CAKUT) are a frequent cause of renal failure in children, and their detection in utero is now common with fetal screening ultrasonography. The clinical course of CAKUT detected before birth is very heterogeneous and dep...

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Detalhes bibliográficos
Main Authors: Madariaga, Leire, Morinière, Vincent, Jeanpierre, Cécile, Bouvier, Raymonde, Loget, Philippe, Martinovic, Jelena, Dechelotte, Pierre, Leporrier, Nathalie, Thauvin-Robinet, Christel, Jensen, Uffe Birk, Gaillard, Dominique, Mathieu, Michele, Turlin, Bruno, Attie-Bitach, Tania, Salomon, Rémi, Gübler, Marie-Claire, Antignac, Corinne, Heidet, Laurence
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Nephrology 2013
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Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3700697/
https://ncbi.nlm.nih.gov/pubmed/23539225
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2215/CJN.10221012
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