Polycystic liver disease (PLD) is a group of genetic disorders characterized by progressive
development of cholangiocyte-derived fluid-filled hepatic cysts. PLD is the most common …

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 (PLD) are a group of genetic disorders initiated by mutations in
several PLD-related genes and characterized by the presence of multiple cholangiocyte …

Polycystic liver diseases are genetic disorders characterized by progressive bile duct
dilatation and/or cyst development. The large volume of hepatic cysts causes different …

(ADPLD) or in association with autosomal-dominant polycystic kidney disease (ADPKD) or
autosomal-recessive polycystic kidney disease (ARPKD). PLD is characterized by the …

Polycystic liver diseases (PLD) are inherited disorders of the biliary epithelium, caused by
genetic defects in proteins associated with intracellular organelles, mainly the endoplasmic …

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

Polycystic liver diseases (PLDs) include a heterogeneous group of congenital disorders
inherited as dominant or recessive genetic traits; they are manifested alone or in association …

Polycystic liver diseases (PCLDs) are genetic disorders with heterogeneous etiologies and
a range of phenotypic presentations. PCLD exhibits both autosomal or recessive dominant …

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 …