Home Albumin Infusion Therapy, Another Alternative Treatment in Patients With Congenital Nephrotic Syndrome of the Finnish Type

Background: Congenital nephrotic syndrome of the Finnish type (CNF) is a rare, severe glomerular disease caused by mutations in the NPHS1 gene, which codes for nephrin. It is characterised by massive proteinuria and severe edoema. Progression to end-stage kidney failure occurs during early childhood...

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Detalles Bibliográficos
Autores principales: Serramontmany, Eugènia, Muñoz, Marina, Fernández-Polo, Aurora, Morillo, María, Gómez-Ganda, Laura, Cañete-Ramírez, Carme, Ariceta, Gema
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7841340/
https://www.ncbi.nlm.nih.gov/pubmed/33520897
http://dx.doi.org/10.3389/fped.2020.614535

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7841340/
https://www.ncbi.nlm.nih.gov/pubmed/33520897
http://dx.doi.org/10.3389/fped.2020.614535

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