Clinical profile of autosomal dominant polycystic liver disease

Q Qian, A Li, BF King, PS Kamath, DJ Lager, JH III… - Hepatology, 2003 - Elsevier
Most reports on the natural history, manifestations, and treatment of polycystic liver disease
are based on the disease as it manifests in patients with autosomal dominant polycystic
kidney disease (ADPKD). The purpose of this study was to develop a clinical profile of
isolated autosomal dominant polycystic liver disease (ADPLD) using nonaffected family
members as controls. The study included 146 probands, known affected relatives, and first-
degree relatives of affected individuals. Participants underwent a formalized medical history …