Figure 2
From: Polycystic liver disease: an overview of pathogenesis, clinical manifestations and management
Comprehensive algorithm for diagnosis, management and genetic counseling in PCLD and ADPKD. The diagnostic criteria for PCLD and ADPKD compromises family history and age-related liver or kidney phenotype respectively [64, 66]. PLD therapy is individually decided according to number, distribution and size of hepatic cysts [78]. Genetic counseling has an important role in symptomatic individuals with a positive family history for hepatic and/or renal cystogenesis in order to differentiate PLD and clinical management.