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- W2553522603 abstract "This report describes the clinical course and management of a patient with Loeys–Dietz syndrome (LDS) type 2. In 2003, a 31-year-old male was diagnosed with acute aortic dissection type B; in the following six years he underwent multiple surgical and endovascular aortic procedures at different thoracic and abdominal levels secondary to progressive enlargement of both the non-dissected thoracic aorta and the false lumen distal to the left subclavian artery. LDS is characterized by arterial tortuosity and aneurysms as a result of heterozygous mutations in genes encoding transforming growth factor-b receptor 1 and 2. Further studies are required to establish the proper surgical management." @default.
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- W2553522603 date "2011-01-01" @default.
- W2553522603 modified "2023-09-23" @default.
- W2553522603 title "Case report - Vascular thoracic Familial aortic aneurysm and dissection due to transforming growth factor-b receptor 2 mutation" @default.
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