HEREDITARY APOLIPOPROTEIN A-1-ASSOCIATED CARDIAC AMYLOIDOSIS PRESENTING WITH A NOVEL GENETIC MUTATION

The diagnosis of rare types of cardiac amyloidosis (CA) is commonly missed or delayed. We present a case of a 55-year-old Caucasian man who presented with worsening dyspnea and peripheral edema for 3 months. He had very low HDL and only mildly elevated levels of serum creatinine, ALT, AST, CK,