Polycystic Kidney and Liver Disease Report

Polycystic Kidney and Liver DiseasePolycystic kidney disease (PKD) is a hereditary condition characterized by the formation of aggregates of cysts in the kidney, variable in size, but capable of compromising excretory function over time. These cysts, non-cancerous formations composed of fluid, can also affect the liver or other body areas. The underlying causes are genetic in nature and involve both the autosomal dominant and recessive patternsmore than 20 genes analyzed It is recommended if: This panel is ideal for patients suspected to have autosomal dominant or autosomal recessive polycystic kidney disease. List of main conditions: Polycystic liver disease 3 with or without kidney cysts Polycystic kidney disease 5 Polycystic kidney disease 4, with or without hepatic disease