Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00035024.xml
Thromb Haemost 2015; 114(04): 859-861
DOI: 10.1160/TH15-01-0040
DOI: 10.1160/TH15-01-0040
Letters to the Editor
A novel mutation of antithrombin deficiency in six family siblings and the clinical combat
Further Information
Publication History
Received:
15 January 2015
Accepted after major revision:
16 April 2015
Publication Date:
29 November 2017 (online)
-
References
- 1 Kenet G, Lutkhoff LK, Albisetti M. et al. Impact of thrombophilia on risk of arterial ischemic stroke or cerebral sinovenous thrombosis in neonates and children: a systematic review and meta-analysis of observational studies. Circulation 2010; 121: 1838-1847.
- 2 Calcaterra D, Martin JT, Ferneini AM. et al. Acute mesenteric and aortic thrombosis associated with antithrombin deficiency: a rare occurrence. Ann Vasc Surg 2010; 24: 415e5-7.
- 3 Tu CM, Hsueg CH, Chu KM. et al. Simultaneous thromboses of double coronary arteries in a young male with antithrombin III deficiency. Am J Emerg Med 2009; 27: 1169e3-6.
- 4 Roldan V, Ordonez A, Marin F. et al. Antithrombin Cambridge II (A384S) supports a role for anti-thrombin deficiency in arterial thrombosis. Thromb Haemost 2009; 101: 483-486.
- 5 Corral J, Hernandez-Espinosa D, Soria JM. et al. Antithrombin Cambridge II (A384S): an underestimated genetic risk factor for venous thrombosis. Blood 2007; 109: 4258-4263.
- 6 Zeng W, Tang L, Jian XR. et al. Genetic analysis should be included in clinical practice when screening for antithrombin deficiency. Thromb Haemost 2015; 113: 262-271.