Cardiac amyloidosis is a rare condition characterized by the abnormal accumulation of proteins in organs like the heart, liver, and kidneys. In the heart, this can lead to thickening of the heart wall and disrupt heart function, causing irregular heart rhythms. Genetic factors, particularly in African American populations, increase the risk of developing heart disease, including cardiac amyloidosis. Lifestyle changes, medication, and expert medical treatment are essential for managing the condition. Early diagnosis is crucial, and tests like biopsies and MRIs can help determine the type of amyloidosis present. Specialized clinics, like the one at Mayo Clinic, offer comprehensive care for individuals with cardiac amyloidosis.
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Expert explains cardiac amyloidosis
