• The panel for hereditary Cardiac Diseases covers 156 genes. All of these genes are sequenced simultaneously. Only genes which have an association with the phenotype of the patient will be interpreted. For diagnostic purposes, each of the gene sets can be requested individually or in combination. A combination of individual genes is also possible.
    • Congenital heart defects
    • Cardiomyopathy (dilated, hypertrophic, restrictive, LV non-compaction)
    • Atrial fibrillation
    • Short and Long QT syndrome
    • Arrhythmogenic RV dysplasia
    • Brugada syndrome
    • CPVT
    • RASopathies
    • Aortic aneurysm / Loeys-Dietz syndrome / Arterial tortuosity syndrome