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

• Main Authors: Aboutarik Fatima Ezzahra (Author), Dassouli Cherihane (Author), Ait Errami Adil (Author), Oubaha Sofia (Author), Samlani Zouhour (Author), Krati Khadija (Author)
• 格式: 圖書
• 出版: Archives of Clinical Gastroenterology - Peertechz Publications, 2022-10-29.
• 主題: Case Report
• 在線閱讀: 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...