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Molecular causes of congenital anomalies of the kidney and urinary tract (CAKUT)

Congenital anomalies of the kidney and urinary tract (CAKUT) occur in 0.5–1/100 newborns and as a group they represent the most frequent cause for chronic kidney failure in children. CAKUT comprise clinically heterogeneous conditions, ranging from mild vesicoureteral reflux to kidney aplasia. Most f...

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Bibliografiske detaljer
Udgivet i:Mol Cell Pediatr
Main Authors: Kohl, Stefan, Habbig, Sandra, Weber, Lutz T., Liebau, Max C.
Format: Artigo
Sprog:Inglês
Udgivet: Springer Berlin Heidelberg 2021
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7904997/
https://ncbi.nlm.nih.gov/pubmed/33625646
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40348-021-00112-0
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