Three Novel Mutations in FBN1 and TGFBR2 in Patients with the Syndromic Form of Thoracic Aortic Aneurysms and Dissections
Author:
Affiliation:
1. Center for Medical Genetics, School of Life Sciences, Central South University
Publisher
International Heart Journal (Japanese Heart Journal)
Subject
Cardiology and Cardiovascular Medicine,General Medicine
Link
https://www.jstage.jst.go.jp/article/ihj/59/5/59_18-046/_pdf
Reference31 articles.
1. 1. Leutermann R, Sheikhzadeh S, Brockstädt L, et al. A 1-bp duplication in TGFB2 in three family members with a syndromic form of thoracic aortic aneurysm. Eur J Hum Genet 2014; 22: 944-8.
2. 2. Miyahara S, Okita Y. Overview of current surgical strategies for aortic disease in patients with Marfan syndrome. Surg Today 2016; 46: 1006-18.
3. 3. Xie GP, Song HJ, Jiang N, et al. Periosteal osteosarcoma and Marfan's syndrome: A case report and literature review. Oncol Lett 2016; 11: 311-5.
4. 4. Loeys BL, Dietz HC, Braverman AC, et al. The revised Ghent nosology for the Marfan syndrome. J Med Genet 2010; 47: 476-85.
5. 5. Suzuki JI, Imai Y, Aoki M, et al. Periodontitis may deteriorate sinus of valsalva dilatation in Marfan syndrome patients. Int Heart J 2016; 57: 456-60.
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