Table 1.
Main clinical manifestation based on refs [1, 3, 6, 12–15] | |
– most frequent presenting feature: acute aortic dissection | |
– Stanford type A dissection more common (54% @ median age 36 yrs) than type B (21% @ median age 27 yrs) | |
– 15–57% @ aortic diameter < 5 cm (often in peri-partum period) | |
– Age dependent occurrence of aortic dissection ○ Rare/absent in children ○ Cumulative risk for aortic event (aortic dissection or surgical aneurysm repair) @85y: 76% | |
– aortic events more prevalent in males (62%) than in females (38%); p = 0.003 | |
– Risk aortic event higher with pathogenic variants affecting the Arg179 and Arg258 residue, lower with p.(Arg185Gln) and p.(Arg118Gln) pathogenic variants | |
– 6% of pregnancies complicated by aortic dissection (third trimester of shortly after delivery) | |
Other clinical features | |
– Occlusive vascular disease | |
○ Premature coronary artery disease (youngest @28 yrs) ○ Moya-Moya like cerebrovascular disease – more common with pathogenic variant affecting the Arg258 residue | |
– Congenital Heart Disease | |
○ Persistent ductus arteriosus (10%) ○ Bicuspid aortic valve (4%) ○ Atrial septal defect | |
– Iris Flocculi (iris cysts at the pupillary border) – more common with p.(Arg149Cys) variant | |
– Livedo reticularis |