Please use this identifier to cite or link to this item:
|Title:||Familial thoracic aortic dilation and bicommissural aortic valve: A prospective analysis of natural history and inheritance|
Bicommissural aortic valve
Left outflow tract
|Citation:||Loscalzo, M.L., Goh, D.L.M., Loeys, B., Kent, K.C., Spevak, P.J., Dietz, H.C. (2007-09-01). Familial thoracic aortic dilation and bicommissural aortic valve: A prospective analysis of natural history and inheritance. American Journal of Medical Genetics, Part A 143 (17) : 1960-1967. ScholarBank@NUS Repository. https://doi.org/10.1002/ajmg.a.31872|
|Abstract:||The autosomal dominant inheritance of bicommissural aortic valve (BAV) (Online Mendelian Inheritance in Man #109730) in some families is well-documented; however, the inheritance of BAV with thoracic aortic aneurysm (TAA) is less clear. Whether the aneurysm is secondary to hemodynamic perturbation related to the valve abnormality or a primary manifestation of the disorder remains controversial. Guidelines are needed regarding the follow-up and treatment of these patients and their families. Thirteen families with at least one individual with TAA and BAV (BAV/TAA) were evaluated prospectively by standard echocardiographic methods or clinical history. Affected status was determined by the presence of BAV or TAA or a history of dissection, rupture, or surgical repair. Six of 13 families had at least two family members with both BAV and TAA, often in successive generations. Informatively, all 13 families had at least one family member with TAA in the absence of BAV. Thirty-five percent (39/110) of family members had BAV/TAA or TAA, and the majority of families (11/13) had maximal dilatation above the sinotubular junction (STJ). Vascular dissection or rupture occurred in seven of 13 families and in individuals with structurally normal aortic valves. Two families had non-manifesting, obligate carriers. Three families have members with other left heart outflow tract anomalies. This study confirms autosomal dominant inheritance with incomplete penetrance for BAV/TAA in these families. Furthermore, our data suggest that the component features, BAV and TAA, are independent manifestations of a single gene defect. To avoid the risk of early death, it is essential that all first-degree relatives receive echocardiographic follow-up at regular intervals regardless of the presence or absence of a BAV. This assessment must include imaging of the aortic region above the STJ. © 2007 Wiley-Liss, Inc.|
|Source Title:||American Journal of Medical Genetics, Part A|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
checked on Sep 21, 2018
WEB OF SCIENCETM
checked on Sep 11, 2018
checked on Aug 16, 2018
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.