Overview
AApoAII amyloidosis is a rare, inherited form of amyloidosis caused by mutations in the apolipoprotein AII (APOAI I) gene. It is characterized by the deposition of amyloid fibrils composed of apolipoprotein AII in various organs, leading to organ dysfunction.Diagnosis
Management
Special Populations
Key Recommendations
References
1 Jin M, Meng F, Yang W, Liang L, Wang H, Fu Z. Efficacy and Safety of Evinacumab for the Treatment of Hypercholesterolemia: A Meta-Analysis. Journal of cardiovascular pharmacology 2021. link 2 Chan FKL, Goh KL, Reddy N, Fujimoto K, Ho KY, Hokimoto S et al.. Management of patients on antithrombotic agents undergoing emergency and elective endoscopy: joint Asian Pacific Association of Gastroenterology (APAGE) and Asian Pacific Society for Digestive Endoscopy (APSDE) practice guidelines. Gut 2018. link