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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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Detalhes bibliográficos
Publicado no:Clin Kidney J
Main Authors: De Rechter, Stéphanie, Bammens, Bert, Schaefer, Franz, Liebau, Max C, Mekahli, Djalila
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2018
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6295604/
https://ncbi.nlm.nih.gov/pubmed/30581562
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/ckj/sfy088
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