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Article

Determinants of renal disease variability in ADPKD.

Advances in chronic kidney disease - 1 Mar 2010

Harris Peter C, Rossetti Sandro

Abstract excerpt

In common with other Mendelian diseases, the presentation and progression of autosomal dominant polycystic kidney disease (ADPKD) vary widely in the population. The typical course is of adult-onset disease with ESRD in the 6th decade. However, a small proportion has adequate renal function into the 9th decade, whereas others present with enlarged kidneys as neonates. ADPKD is genetically heterogeneous, and the...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Share to Polycystic Kidney, Autosomal Dominant

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Source

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Identifiers

PMID: 20219616
DOI: 10.1053/j.ackd.2009.12.004
PMCID: PMC2837603

Genes

PKD1
PKD2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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