Literature DB >> 31085000

Familial Spontaneous Coronary Artery Dissection and the SMAD-3 Mutation.

Amir Solomonica1, Rodrigo Bagur1, Tawfiq Choudhury1, Shahar Lavi2.   

Abstract

Spontaneous coronary artery dissection (SCAD) is a cause of about 4% of acute coronary syndrome. The pathophysiology of SCAD is not yet fully understood. Loeys-Dietz syndrome is a connective tissue disorder characterized by aortic aneurysms, arterial tortuosity, and aortic dissections. It is caused by mutations in the genes affecting the transforming growth factor β pathway. We describe a family with a SMAD3 gene mutation and Loeys-Dietz syndrome presenting with recurrent SCAD episodes.
Copyright © 2019 Elsevier Inc. All rights reserved.

Entities:  

Year:  2019        PMID: 31085000     DOI: 10.1016/j.amjcard.2019.04.035

Source DB:  PubMed          Journal:  Am J Cardiol        ISSN: 0002-9149            Impact factor:   2.778


  3 in total

1.  Genome-Wide Identification of Associations of Circulating Molecules With Spontaneous Coronary Artery Dissection and Aortic Aneurysm and Dissection.

Authors:  Tianci Chai; Mengyue Tian; Xiaojie Yang; Zhihuang Qiu; Xinjian Lin; Liangwan Chen
Journal:  Front Cardiovasc Med       Date:  2022-04-27

2.  Association of Circulating Cathepsin B Levels With Blood Pressure and Aortic Dilation.

Authors:  Tianci Chai; Mengyue Tian; Xiaojie Yang; Zhihuang Qiu; Xinjian Lin; Liangwan Chen
Journal:  Front Cardiovasc Med       Date:  2022-03-29

Review 3.  Cardiovascular disease in women: A review of spontaneous coronary artery dissection.

Authors:  Bashar Khiatah; Sam Jazayeri; Naofumi Yamamoto; Tristen Burt; Amanda Frugoli; Dennis L Brooks
Journal:  Medicine (Baltimore)       Date:  2022-09-23       Impact factor: 1.817

  3 in total

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