Polycystic kidney disease (PKD) is a genetic disorder characterized by the formation of numerous cysts in the kidneys. There are various synonyms that can be used to describe this condition including autosomal dominant polycystic kidney disease (ADPKD), familial cystic disease of the kidneys, and Potter syndrome type three. ADPKD is the most common type of PKD and is inherited in an autosomal dominant manner. Symptoms of PKD include abdominal pain, high blood pressure, and kidney failure. Treatment options vary depending on the severity of the condition and may include medications, surgery, or dialysis. It is important for individuals with PKD to receive proper medical care and monitoring.