From Uncertainty to Accuracy: Optimizing Outcomes in Adult Genetic Cholestatic Liver Diseases
Description
Progressive familial intrahepatic cholestasis (PFIC) and Alagille syndrome (ALGS) frequently present diagnostic challenges in adult clinical practice due to variable phenotypes, delayed recognition, and overlapping hepatic and extrahepatic manifestations. Key focus areas include diagnostic evaluation strategies to recognize previously undiagnosed or later-presenting disease in adults, characterization of hepatic and extrahepatic complications, and implementation of coordinated interprofessional care models. Additionally, evidence-based approaches for selecting targeted management strategies address bile acid accumulation, severe pruritus, and long-term hepatic outcomes. Interactive case-based analysis illustrates essential decision points to optimize clinical recognition, disease monitoring, and overall patient management.
- CE: 1.25 CME Hours
- Supported by: Mirum Pharmaceuticals
- Organized by: Medscape Education
- For more information and to register, visit: www.medscape.org/symposium/liver-disease-genetics
