Your Trusted Leader in Cardiac Amyloidosis Care
Our heart experts take a multidisciplinary approach to treat cardiac amyloidosis. You can count on us to design a comprehensive care plan that includes an accurate diagnosis, personalized therapy options, and access to innovative clinical trials.
Overview
Cardiac amyloidosis is a rare and potentially life-threatening condition. It happens when misshapen proteins (amyloids) collect in your heart. Your heart muscle thickens and stiffens. As a result, it struggles to pump blood throughout your body.
There are two main types of cardiac amyloidosis:
- Light Chain Amyloidosis (AL)—abnormal proteins from bone marrow fold incorrectly and collect in your heart and other organs. AL may be linked to the blood cancer multiple myeloma.
- Transthyretin Amyloidosis (ATTR)—abnormal proteins from the liver fold incorrectly and potentially cause heart failure in older adults. You may inherit this type of cardiac amyloidosis or it can occur naturally during aging.
When left untreated, cardiac amyloidosis may cause serious complications, including:
- Arrhythmia, such as atrial fibrillation (AFib)
- Heart failure
- Kidney failure
- Stroke
- Sudden cardiac death


