The full spectrum of phenotypes associated with some genes of the TGF‐β related vasculopathies, such as FBN1 and TGFBR1/2, has been described extensively (Arslan‐Kirchner et al., 2011; Cook, Carta, Galatioto, & Ramirez, 2015; Lerner‐Ellis et al., 2014; Ramachandra et al., 2015; Romaniello et al., 2014). This evidence concerns the gene FBN1 and vascular disorder.