A Case of Alport Syndrome Associated with Recurrent Stanford Type B Aortic Dissections
Author:
Affiliation:
1. Department of Cardiovascular Surgery, Tohoku Medical and Pharmaceutical University
Publisher
The Editorial Committee of Annals of Vascular Diseases
Subject
Pharmaceutical Science
Link
https://www.jstage.jst.go.jp/article/avd/15/2/15_cr.22-00010/_pdf
Reference7 articles.
1. 1) Nozu K, Nakanishi K, Abe Y, et al. A review of clinical characteristics and genetic backgrounds in Alport syndrome. Clin Exp Nephrol 2019; 23: 158-68.
2. 2) Borza D-B, Bondar O, Ninomiya Y, et al. The NC1 domain of collagen IV encodes a novel network composed of the alpha 1, alpha 2, alpha 5, and alpha 6 chains in smooth muscle basement membranes. J Biol Chem 2001; 276: 28532-40.
3. 3) Kashtan CE, Segal Y, Flinter F, et al. Aortic abnormalities in males with Alport syndrome. Nephrol Dial Transplant 2010; 25: 3554-60.
4. 4) Lyons OTA, St. John ERC, Morales JP, et al. Ruptured thoracoabdominal aortic aneurysm in a renal transplant patient with Alport’s syndrome. Ann Vasc Surg 2007; 21: 816-8.
5. 5) Vogt BA, Birk PE, Panzarino V, et al. Aortic dissection in young patients with chronic hypertension. Am J Kidney Dis 1999; 33: 374-8.
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