Interestingly, LGE is rare in patients with low-risk genetic variants, while patients with variants at greater arrhythmic risks present more typical patterns: DSP, FLNC, and PLN with a predominance of LGE subepicardial ring-like scar pattern, LMNA with a mid-wall basal, or septal LGE distribution, whereas titin (TTN), BAG cochaperone-3 (BAG3), duchenne muscular dystrophy (DMD), RBM20, and some form of LMNA genotypes show unspecific or heterogeneous LGE patterns [13,64,65,66]. The gene discussed is TTN; the disease is Duchenne muscular dystrophy.