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Analysis of multigenerational families with thoracic aortic aneurysms and dissections due to TGFBR1 or TGFBR2 mutations

✍ Scribed by Tran-Fadulu, V. (author);Pannu, H. (author);Kim, D. H. (author);Vick, G. W. (author);Lonsford, C. M. (author);Lafont, A. L. (author);Boccalandro, C. (author);Smart, S. (author);Peterson, K. L. (author);Zenger Hain, J. (author);Willing, M. C. (author);Coselli, J. S. (author);LeMaire, S. A. (author);Ahn, C. (author);Byers, P. H. (author);Milewicz, D. M. (author)

Book ID
121750426
Publisher
BMJ Publishing Group
Year
2009
Tongue
English
Weight
480 KB
Volume
46
Category
Article
ISSN
0022-2593

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Approximately 20% of aortic aneurysm and/or dissection (AAD) cases result from inherited disorders, including several systemic and syndromatic connective-tissue disorders, such as Marfan syndrome, Ehlers-Danlos syndrome, and Loeys-Dietz syndrome, which are caused by mutations in the FBN1, COL3A1, an