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

• Autors principals: Aboutarik Fatima Ezzahra (Autor), Dassouli Cherihane (Autor), Ait Errami Adil (Autor), Oubaha Sofia (Autor), Samlani Zouhour (Autor), Krati Khadija (Autor)
• Format: Llibre
• Publicat: Archives of Clinical Gastroenterology - Peertechz Publications, 2022-10-29.
• Matèries: Case Report
• Accés en línia: 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...