Polycystic liver disease: Classification, diagnosis, treatment process, and clinical management

Table 1 Brief summary of various polycystic liver disease

Disease	Genes mutation	Kidney involvement
ADPKD	PKD1, PKD2, GANAB	Yes
ARPKD	PKHD1	Yes
PCLD	PRKCSH, SEC63, LRP5, GANAB, ALG8, SEC61B, PKHD1	Usually not

ADPKD: Autosomal dominant polycystic kidney disease; ARPKD: Autosomal recessive polycystic kidney disease; PCLD: Isolated polycystic liver disease.