Modelling polycystic liver disease progression using age-adjusted liver volumes and targeted mutational analysis

Background & Aims: Polycystic liver disease (PLD) manifests as numerous fluid-filled cysts scattered throughout the liver parenchyma. PLD most commonly develops in females, either as an extra-renal manifestation of autosomal-dominant polycystic kidney disease (ADPKD) or as isolated autosomal...

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Bibliographic Details

Published in:	JHEP Reports
Main Authors:	Dana Sierks, Ria Schönauer, Anja Friedrich, Elena Hantmann, Jonathan de Fallois, Nikolas Linder, Janett Fischer, Adam Herber, Carsten Bergmann, Thomas Berg, Jan Halbritter
Format:	Article
Language:	English
Published:	Elsevier 2022-11-01
Subjects:	polycystic disease polycystic kidney disease ADPLD ADPKD PCLD PLD
Online Access:	http://www.sciencedirect.com/science/article/pii/S2589555922001513