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Updated: May 27, 2026

A Pipeline to Characterize Structural Heart Defects in the Fetal Mouse
08:19

A Pipeline to Characterize Structural Heart Defects in the Fetal Mouse

Published on: December 16, 2022

新生児の巨型室内左心室性ラブドミオマ

Massimo A Padalino1, Vladimiro L Vida, Anil Bhattarai

  • 1Pediatric and Congenital Cardiac Surgery Unit, Centro "V. Gallucci," Padova, Italy. massimo.padalino@unipd.it

Circulation
|November 16, 2011
PubMed
まとめ

No abstract available in PubMed .

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Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...