Given the involvement of increased TGFβ ligand in Marfan syndrome, it is not surprising to find that mutations in other components of the TGFβ pathway can result in related disorders, collectively termed MFS-like syndromes [3–5], including Marfan syndrome 2 (MFS2), Loeys-Dietz syndrome (LDS), Ehlers-Danlos syndrome (LDS-2), Thoracic Aortic Aneurysms and Dissections (TAAD) and Shprintzen-Goldberg syndrome (SGS). The gene discussed is TGFB1; the disease is Rare disease with thoracic aortic aneurysm and aortic dissection.