Recent Progress of the ARegPKD Registry Study on Autosomal Recessive Polycystic Kidney Disease

Autosomal recessive polycystic kidney disease (ARPKD) is a rare monogenic disease with a severe phenotype often presenting prenatally or in early childhood. With its obligate renal and hepatic involvement, ARPKD is one of the most important indications for liver and/or kidney transplantation in chil...

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Detalles Bibliográficos
Autores principales: Ebner, Kathrin, Schaefer, Franz, Liebau, Max Christoph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5327862/
https://www.ncbi.nlm.nih.gov/pubmed/28296980
http://dx.doi.org/10.3389/fped.2017.00018

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5327862/
https://www.ncbi.nlm.nih.gov/pubmed/28296980
http://dx.doi.org/10.3389/fped.2017.00018

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