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Thromb Haemost 2015; 113(03): 668-670
DOI: 10.1160/TH14-11-0913
DOI: 10.1160/TH14-11-0913
Letters to the Editor
Recurrent spontaneous coronary dissections in a patient with a de novo fibrillin-1 mutation without Marfan syndrome
Authors
Financial support: This research was supported by Deutsche Forschungs - gemeinschaft (DFG SFB 1123-A1/A2 to P. v. H./C. W.), the European Research Council (ERC Advanced Grant 249929 to C. W.), and the Leducq Network CVGeneF(x).
Further Information
Publication History
Received:
04 November 2014
Accepted after major revision:
07 November 2014
Publication Date:
17 November 2017 (online)
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References
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- 2 Loeys BL, Dietz HC, Braverman AC. et al. The revised Ghent nosology for the Marfan syndrome. J Med Genet 2010; 47: 476-485.
- 3 Grond-Ginsbach C, Pjontek R, Aksay SS, Hyhlik-Durr A, Bockler D, Gross-Weissmann ML. Spontaneous arterial dissection: phenotype and molecular pathogenesis. Cell Mol Life Sci 2010; 67: 1799-1815.
- 4 Daniel JM, Sedding DG. Circulating smooth muscle progenitor cells in arterial remodeling. J Mol Cell Cardiol 2011; 50: 273-279.
- 5 Rybczynski M, Bernhardt AMJ, Rehder U. et al. The spectrum of syndromes and manifestations in individuals screened for suspected Marfan syndrome. Am J Med Genet Part A 2008; 146A: 3157-3166.
- 6 Exome Aggregation Consortium (ExAC), Cambridge, MA, USA. Available at: http://exac.broa-dinstitute.org . Accessed November 14, 2014.