Early clinical management of autosomal recessive polycystic kidney disease

Autosomal recessive polycystic kidney disease (ARPKD) is a rare but highly relevant disorder in pediatric nephrology. This genetic disease is mainly caused by variants in the PKHD1 gene and is characterized by fibrocystic hepatorenal phenotypes with major clinical variability. ARPKD frequently prese...

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Detalles Bibliográficos
Autor principal: Liebau, Max Christoph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Educational Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8497312/
https://www.ncbi.nlm.nih.gov/pubmed/33594464
http://dx.doi.org/10.1007/s00467-021-04970-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8497312/
https://www.ncbi.nlm.nih.gov/pubmed/33594464
http://dx.doi.org/10.1007/s00467-021-04970-8

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