Unusual hypertrophic cardiomyopathy: case report of an early onset wild-type ATTR amyloidosis accompanied by a chromosomal duplication involving the MYH6 and MYH7 gene

BackgroundHypertrophic cardiomyopathy (HCM) is characterized by an increased left ventricular (LV) wall thickness and LV mass. With an estimated prevalence of 1:200–500, HCM is among the most common genetically determined cardiac diseases. Functionally, enhanced tissue stiffness and reduced elastici...

Description complète

Détails bibliographiques

Auteurs principaux:	Jassin Hamidi, Yvonne Hanel, Sven Dittmann, Wanda Maria Gerding, Huu Phuc Nguyen, Karin Klingel, Eric Schulze-Bahr
Format:	Artigo
Langue:	Inglês
Publié:	Frontiers Media S.A. 2025-02-01
Collection:	Frontiers in Cardiovascular Medicine
Sujets:	hypertrophic cardiomyopathy wtATTR amyloidosis copy number variation MYH6 MYH7
Accès en ligne:	https://www.frontiersin.org/articles/10.3389/fcvm.2025.1462523/full
Tags:	Ajouter un tag Pas de tags, Soyez le premier à ajouter un tag!