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Updated: Jun 3, 2026

Genetic Analysis of Hereditary Transthyretin Ala97Ser Related Amyloidosis
Published on: June 9, 2018
[Familial approach in hereditary transthyretin cardiac amyloidosis]
Pablo García-Pavía1, Patricia Avellana, Belén Bornstein
1Unidad de Miocardiopatías, Sección de Trasplante Cardiaco, Servicio de Cardiología, Hospital Universitario Puerta de Hierro, Majadahonda, Madrid, España. pablogpavia@yahoo.es
Abstract:
Cardiac amyloidosis is a disease of complex diagnosis and treatment. Some subtypes of cardiac amyloidosis are inherited. Among these, the most common variant is caused by mutations in the transthyretin gene. Correct identification of amyloidosis produced by a genetic defect is of great importance because it modifies the diagnostic and therapeutic approach in patients and their families. We describe our experience in the evaluation of two families with hereditary transthyretin cardiac amyloidosis. We discuss a number of considerations related to the evaluation of these patients and the diagnostic and therapeutic approach to perform in relatives.
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