Successful Surgical Repair of Type A Acute Aortic Dissection in a Patient with Vascular Ehlers–Danlos Syndrome
Author:
Affiliation:
1. Department of Cardiovascular Surgery, Faculty of Medicine, University of Miyazaki
Publisher
The Editorial Committee of Annals of Vascular Diseases
Link
https://www.jstage.jst.go.jp/article/avd/15/1/15_cr.21-00122/_pdf
Reference9 articles.
1. 1) Malfait F, Francomano C, Byers P, et al. The 2017 international classification of the Ehlers–Danlos syndromes. Am J Med Genet C Semin Med Genet 2017; 175: 8-26.
2. 2) Oderich GS, Panneton JM, Bower TC, et al. The spectrum, management and clinical outcome of Ehlers–Danlos syndrome type IV: a 30-year experience. J Vasc Surg 2005; 42: 98-106.
3. 3) Pepin MG, Schwarze U, Rice KM, et al. Survival is affected by mutation type and molecular mechanism in vascular Ehlers–Danlos syndrome (EDS type IV). Genet Med 2014; 16: 881-8.
4. 4) Frank M, Albuisson J, Ranque B, et al. The type of variants at the COL3A1 gene associates with the phenotype and severity of vascular Ehlers–Danlos syndrome. Eur J Hum Genet 2015; 23: 1657-64.
5. 5) Conte S, Serraf A, Lacour-Gayet F, et al. Successful repair of thoracic aortic aneurysm in a child with Ehlers–Danlos syndrome. J Thorac Cardiovasc Surg 1997; 113: 410-1.
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1. Genetic Basis, New Diagnostic Approaches, and Updated Therapeutic Strategies of the Syndromic Aortic Diseases: Marfan, Loeys–Dietz, and Vascular Ehlers–Danlos Syndrome;International Journal of Environmental Research and Public Health;2023-08-20
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