A rare liver disease characterized by immune-mediated acute or chronic liver inflammation clinically presenting as cryptogenic hepatitis with interface hepatitis on histological examination elevated serum aminotransferase levels and hypergammaglobulinemia / elevated immunoglobulin G in the presence or absence of specific circulating autoantibodies. Patients may be asymptomatic chronically ill or present with acute liver failure. Concurrent autoimmune diseases are frequently observed.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http: //www.orphadata.org. Data version October 2023.
Newly diagnosed with
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Global Liver Institute
To improve the lives of individuals and families impacted by liver disease through promoting innovation, encouraging collaboration, and scaling optimal approaches to help eradicate liver diseases.
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