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Updated: Jul 1, 2025
Genetic Analysis of Hereditary Transthyretin Ala97Ser Related Amyloidosis
Published on: June 9, 2018
Coexistence of Light Chain and Transthyretin Cardiac Amyloidosis
Abhishek Gami1, John Woller1, Paul Scheel2
1Department of Internal Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Abstract:
Although most patients with cardiac amyloidosis are diagnosed with either light chain (AL) or transthyretin (ATTR) disease, coexisting amyloid subtypes can occur. We present three cases of coexisting AL and ATTR cardiac amyloidosis and demonstrate the importance of clinical history and endomyocardial biopsy in diagnosis of this rare entity.
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