Polycystic liver disease (PLD) is a clinical condition characterized by the presence of more
than 10 cysts in the liver. It is a rare disease Of genetic etiology that presents as an isolated …

Polycystic liver disease (PLD) is a rare hereditary disease that independently exists in
isolated PLD, or as an accompanying symptom of autosomal dominant polycystic kidney …

Polycystic liver disease (PLD) is arbitrarily defined as a liver that contains> 20 cysts. The
condition is associated with two genetically distinct diseases: as a primary phenotype in …

Polycystic liver disease (PLD) is the result of embryonic ductal plate malformation of the
intrahepatic biliary tree. The phenotype consists of numerous cysts spread throughout the …

Polycystic liver disease rarely occurs in isolation as part of autosomal dominant polycystic
liver disease, but more commonly, it exists as an extra-renal manifestation of autosomal …

Polycystic liver diseases (PLD) represent a group of genetic disorders in which cysts occur
in the liver (autosomal dominant polycystic liver disease) or in combination with cysts in the …

Introduction: Polycystic liver disease (PLD) is characterized by the presence of multiple
cholangiocyte-derived hepatic cysts that progressively replace liver tissue. They are …

Polycystic liver diseases (PLDs) are inherited genetic disorders characterized by
progressive development of intrahepatic, fluid-filled biliary cysts (more than ten), which …

The focus of this review is polycystic liver disease, a genetic disorder characterized by
multiple macroscopic liver cysts that initially bud from biliary epithelium but subsequently …

Aliment Pharmacol Ther 2011; 34: 702–713 Summary Background Polycystic liver diseases
(PCLD) represent a group of genetic disorders in which cysts occur solely in the liver, or …