
Cardiomyopathies include several heart muscle diseases that are often incompletely defined in terms of cause and pathway and often poorly responsive to the proposed treatment. Even in largely recognized entities as myocarditis, the adoption of the effective therapy is still debated and the agents involved are increasingly identified by the new-generation sequencies technique. In fact, the morphomolecular investigation of endomyocardial biopsy samples appear to be inevitable to obtain a personalized and most effective treatment.
Regarding the origin of cardiac electrical instability, the direct involvement of conduction tissue (CT) is recognizable in endomyocardial biopsies examination and the possibility to explore CT damage through the determination of CT main molecular complex HCN4 in the peripheral blood appear as a likely prospective option. Many rare diseases phenotyipically express as cardiomyopathies and their definition and identification is crucial for appropriate management.
Nevertheless, even the administration of the lacking molecular component (i.e., enzyme replacement therapy—ERT) can be clinically unsatisfactory. Recently, it has been shown that ERT delivery can be limited in Fabry disease cardiomyopathy by a reduced expression of mannose-6-phosphate receptor that provides its uptake at the level of cell membrane as well as its targeting into lysosomes.
The aim of the present webinar is to update the latest morpho-molecular and genetic knowledge in cardiomyopathy.
Date: 11 December 2025
Time: 2:00 pm CET | 8:00 am EST | 9:00 pm CST Asia
Webinar ID: 875 7695 1210
Webinar Secretariat: journal.webinar@mdpi.com


In this section, you will find the recordings of this webinar to watch, re-watch and share with your colleagues!
"Morpho-Molecular and Genetic Basis of Cardiomyopathies"
Edited by Prof. Dr. Andrea Frustaci
Deadline for manuscript subissions: 30 June 2026