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Cardiac amyloidosis: Treatment and prognosis - UpToDate Amyloid deposits can occur in a variety of organs, but morbidity and mortality from amyloid deposition most commonly occur when the heart, kidney, liver, or autonomic nervous system are affected (See "Overview of amyloidosis" ) This topic will review the treatment and prognosis of cardiac amyloidosis
Cardiac Amyloidosis Clinic - Overview - Mayo Clinic A team approach At the Cardiac Amyloidosis Clinic, doctors who specialize in blood conditions (hematologists), the heart (cardiologists), imaging (radiologists), anatomic pathology, computational biology, neurology, nephrology and hypertension, and other areas work together to provide excellent, comprehensive care
FOCUS on Cardiac Amyloidosis - European Society of Cardiology Cardiac amyloidosis is a progressive disease caused by the extracellular deposition of amyloid fibrils in the heart More frequent than previously believed, it contributes to many common clinical scenarios such as severe aortic stenosis, increased left ventricular wall thickness and heart failure with preserved ejection fraction
Cardiac amyloidosis | Cardiomyopathy UK How is cardiac amyloidosis diagnosed? Diagnosis can take time, as many people present with symptoms of heart failure, which are treated, while the underlying cause may be difficult to identify Investigations may include blood tests, an echocardiogram, an electrocardiogram (ECG), a cardiac MRI scan, and a DPD scan (a special scan that uses a tracer to detect amyloid in the heart) Genetic