PKD2-Related Autosomal Dominant Polycystic Kidney Disease: Prevalence, Clinical Presentation, Mutation Spectrum, and Prognosis

BACKGROUND: PKD2-related autosomal dominant polycystic kidney disease (ADPKD) is widely acknowledged to be of milder severity than PKD1-related disease, but population-based studies depicting the exact burden of the disease are lacking. We aimed to revisit PKD2 prevalence, clinical presentation, mut...

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Detaylı Bibliyografya
Yayımlandı:Am J Kidney Dis
Asıl Yazarlar: Gall, Emilie Cornec-Le, Audrézet, Marie-Pierre, Renaudineau, Eric, Hourmant, Maryvonne, Charasse, Christophe, Michez, Eric, Frouget, Thierry, Vigneau, Cécile, Dantal, Jacques, Siohan, Pascale, Longuet, Hélène, Gatault, Philippe, Ecotière, Laure, Bridoux, Frank, Mandart, Lise, Hanrotel-Saliou, Catherine, Stanescu, Corina, Depraetre, Pascale, Gie, Sophie, Massad, Michiel, Kersalé, Aude, Séret, Guillaume, Augusto, Jean-François, Saliou, Philippe, Maestri, Sandrine, Chen, Jian-Min, Harris, Peter C., Férec, Claude, Le Meur, Yannick
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2017
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Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5610929/
https://ncbi.nlm.nih.gov/pubmed/28356211
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1053/j.ajkd.2017.01.046
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