Severe polycystic liver disease: An unsual cause of chronic Budd-Chiari Syndrome

• Egile Nagusiak: Aboutarik Fatima Ezzahra (Egilea), Dassouli Cherihane (Egilea), Ait Errami Adil (Egilea), Oubaha Sofia (Egilea), Samlani Zouhour (Egilea), Krati Khadija (Egilea)
• Formatua: Liburua
• Argitaratua: Archives of Clinical Gastroenterology - Peertechz Publications, 2022-10-29.
• Gaiak: Case Report
• Sarrera elektronikoa: Connect to this object online.

<p>Autosomal dominant polycystic kidney disease is a hereditary disease, characterized by the development of cysts in the renal parenchyma with extra-renal manifestations. Liver damage is rarely a source of complications. A Budd-Chiari syndrome could occur following the compression of the supr...