Clinical profile of autosomal dominant polycystic liver disease

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 po...

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Veröffentlicht in:	Hepatology (Baltimore, Md.) Md.), 2003, Vol.37 (1), p.164-171
Hauptverfasser:	Qian, Qi, Li, Airong, King, Bernard F., Kamath, Patrick S., Lager, Donna J., Huston, John, Shub, Clarence, Davila, Sonia, Somlo, Stefan, Torres, Vicente E.
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Aged Biological and medical sciences Child Cysts - diagnostic imaging Cysts - epidemiology Cysts - genetics Cysts - pathology Echocardiography Family Health Gastroenterology. Liver. Pancreas. Abdomen Genes, Dominant Genetic Linkage Humans Liver Diseases - diagnostic imaging Liver Diseases - epidemiology Liver Diseases - genetics Liver Diseases - pathology Liver. Biliary tract. Portal circulation. Exocrine pancreas Magnetic Resonance Imaging Medical sciences Middle Aged Phenotype Prevalence Risk Factors Tumors
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