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...

Descripción completa

Detalles Bibliográficos
Autores principales: Kohl, Stefan, Habbig, Sandra, Weber, Lutz T., Liebau, Max C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Mini Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7904997/
https://www.ncbi.nlm.nih.gov/pubmed/33625646
http://dx.doi.org/10.1186/s40348-021-00112-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7904997/
https://www.ncbi.nlm.nih.gov/pubmed/33625646
http://dx.doi.org/10.1186/s40348-021-00112-0

Ejemplares similares