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Article

ARPKD and early manifestations of ADPKD: the original polycystic kidney disease and phenocopies.

Pediatric nephrology (Berlin, Germany) - 1 Jan 2015

Bergmann Carsten

Abstract excerpt

Renal cysts are clinically and genetically heterogeneous conditions. Polycystic kidney disease (PKD) is common and its characterization has paved the way for the identification of a growing number of cilia-related disorders (ciliopathies) of which most show cystic kidneys. While the recessive form of PKD (ARPKD) virtually always presents in childhood, early onset can, in some instances, also occur in the dominant...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Polycystic Kidney, Autosomal Dominant

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Source

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Identifiers

PMID: 24584572
DOI: 10.1007/s00467-013-2706-2
PMCID: PMC4240914

Genes

PKD1
PKD2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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