Amyloidosis

As the patients with grade 1 DPD uptake had no signs of monoclonal disease, these findings highlight potential early ATTR amyloid cardiomyopathy. Read More ›

Clinicians need to be educated on best practices, to identify and appropriately manage gastrointestinal manifestations as a signal of hereditary amyloidosis. Read More ›

Case study of a 79-year-old African American female, who presented with an exacerbation of congestive heart failure, highlights the importance of diagnosis, treatment, and genetic testing. Read More ›

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