Challenges in preventing sudden cardiac death. The importance of familial background, genetic profiling and follow-up in specialised units.

Early detection of hTTR cardiac amyloidosis with bone DPD scintigraphy in a patient with a rare transthyretin mutation

Alcohol septal ablation in a patient with hypertrophic obstructive cardiomyopathy due to Anderson-Fabry disease

Ventricular hypertrophy in a family with sarcomeric hypertrophic cardiomyopathy: always of genetic origin?

Restrictive cardiomyopathy and anomalous origin of the right coronary artery in a patient with desmin- and myotilin-gene variants: a deleterious combination.