Amyloidosis News - November 2020

The neurologic features of patients with wild-type transthyretin are highlighted, and the variability and overlap of neurologic symptoms are categorized in this case review series. Read Article ›

Focusing on the prevalence of the Val122Ile mutation in African-American patients with hereditary transthyretin cardiac amyloidosis may lead to underestimation of this condition in this population. Read Article ›

This case study highlights the importance of selecting the appropriate imaging modality to diagnose cardiac amyloidosis. Read Article ›

In a select group of patients with transthyretin cardiac amyloidosis (TTR-CA) and heart failure with reduced ejection fraction, guideline-directed medical therapy may be beneficial. Read Article ›

Educating clinicians about transthyretin amyloidosis (ATTR) may help reduce the myriad of challenges and burdens faced by patients with ATTR and their families. Read Article ›

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