Expert opinion on monitoring symptomatic hereditary transthyretin-mediated amyloidosis and assessment of disease progression.
David AdamsVincent AlgalarrondoMichael PolydefkisNitasha SarswatMichel S SlamaJose N NativiPublished in: Orphanet journal of rare diseases (2021)
We suggest that a multisystem approach to monitoring the signs and symptoms of ATTRv amyloidosis best captures the course of the disease. We hope this work will help form the basis of further, consensus-based guidance for the treatment of ATTRv amyloidosis.