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Article

Autosomal dominant polycystic kidney disease in the first year of life. Report of a case with no family history.

Acta urologica Belgica - 1 Dec 1993

Stalens J P, Sokal E, Walon C, Verellen-Dumoulin C, Clapuyt P, Wese F X

Abstract excerpt

Autosomal recessive polycystic kidney disease (RPKD) (also called infantile polycystic kidney disease) and autosomal dominant polycystic kidney disease (DPKD) (or adult form) are the two main types of genetic polycystic kidney diseases (PKD) encountered in children and infants. We report here a case of DPKD with no family history and discuss the main features leading to the differential diagnosis between these...

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PMID: 8296686

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

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