Video Experimental Relacionado

Updated: Sep 10, 2025

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model

Published on: August 8, 2022

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Papel pronóstico de la intensidad del ejercicio en las variantes familiares de truncamiento de la filamina C

Giulio Savonitto1, Alessia Paldino2, Martina Setti1,3

  • 1Cardiothoracovascular Department, Center for Diagnosis and Treatment of Cardiomyopathies, Azienda Sanitaria Universitaria Giuliano-Isontina, University of Trieste; European Reference Network for Rare, Low-Prevalence, and Complex Diseases of the Heart (ERN GUARD-Heart), Trieste, Italy.

Open heart
|August 27, 2025
PubMed
Resumen

El ejercicio de alta intensidad parece seguro para los portadores de la variante truncante de filamina C sin síntomas. Sin embargo, las personas con afecciones cardíacas existentes deben tener precaución, ya que las arritmias que ponen en peligro la vida se produjeron durante la actividad intensa en sujetos afectados.

Palabras clave:
CardiomiopatíasCardiomiopatía dilatadaEnfermedades genéticas, congénitas

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