Wild-type amyloidosis (ATTRwt) progresses slowly, often leading to a better prognosis compared to other types of amyloidosis. Regular doctor visits are crucial to monitor heart function and track disease progression using tests like echocardiograms, imaging, and biomarkers. Life expectancy varies, but many live years after Show Full Answer
Wild-type amyloidosis (ATTRwt) progresses slowly, often leading to a better prognosis compared to other types of amyloidosis. Regular doctor visits are crucial to monitor heart function and track disease progression using tests like echocardiograms, imaging, and biomarkers. Life expectancy varies, but many live years after diagnosis. Discussing treatment options like tafamidis or heart transplants with your doctor can help plan for the future.
February 6, 2025