Unmet needs and challenges for follow-up and treatment of autosomal dominant polycystic kidney disease: the paediatric perspective

Awareness is growing that the clinical course of autosomal dominant polycystic kidney disease (ADPKD) already begins in childhood, with a broad range of both symptomatic and asymptomatic features. Knowing that parenchymal destruction with cyst formation and growth starts early in life, it seems reas...

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Detalles Bibliográficos
Autores principales: De Rechter, Stéphanie, Bammens, Bert, Schaefer, Franz, Liebau, Max C, Mekahli, Djalila
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Reviews
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6295604/
https://www.ncbi.nlm.nih.gov/pubmed/30581562
http://dx.doi.org/10.1093/ckj/sfy088

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6295604/
https://www.ncbi.nlm.nih.gov/pubmed/30581562
http://dx.doi.org/10.1093/ckj/sfy088

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