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C. Röcken

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Case report Open access Sep 2026

Rare Hereditary Cardiac Amyloidosis Treated With SGLT2 Inhibitor

Background Rare hereditary cardiac amyloidosis (CA) may mimic transthyretin or light-chain cardiomyopathy, and reports for effective therapy in these entities are limited. Case Summary A 61-year-old man presented with progressive heart failure (NYHA functional class III). Medical history included bilateral carpal tunne...

J. Voran, Željka Radić, L. Kilian et al. · 0 citations

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