دورية أكاديمية
أعرض في EDS

Spontaneous Coronary Artery Dissection in Females With the Fragile X FMR1 Premutation.

التفاصيل البيبلوغرافية
العنوان: Spontaneous Coronary Artery Dissection in Females With the Fragile X FMR1 Premutation.
المؤلفون: McKenzie FJ; Medical Investigation of Neurodevelopmental Disorders Institute, University of California Davis Medical Center, Sacramento, California.; Department of Psychiatry and Behavioral Sciences, University of California Davis School of Medicine, Sacramento, California., Tassankijpanich N; Division of Developmental and Behavioral Pediatrics, Department of Pediatrics, Faculty of Medicine, Prince of Songkla University, Songkhla, Thailand., Epps KC; Inova Heart and Vascular Institute, Department of Cardiology, Falls Church, Virginia., March SK; University of Minnesota Physicians, Department of Cardiology, Minneapolis, Minnesota., Hagerman RJ; Medical Investigation of Neurodevelopmental Disorders Institute, University of California Davis Medical Center, Sacramento, California.; Department of Pediatrics, University of California Davis School of Medicine, Sacramento, California.
المصدر: JACC. Case reports [JACC Case Rep] 2020 Jan; Vol. 2 (1), pp. 40-44. Date of Electronic Publication: 2020 Jan 15.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Elsevier Inc Country of Publication: Netherlands NLM ID: 101757292 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2666-0849 (Electronic) Linking ISSN: 26660849 NLM ISO Abbreviation: JACC Case Rep Subsets: PubMed not MEDLINE
أسماء مطبوعة: Original Publication: [Amsterdam] : Elsevier Inc., [2019]-
مستخلص: This paper reports 2 cases of female carriers of the FMR1 premutation for developing spontaneous coronary artery dissection (SCAD). These women had classical presentations of premutation symptoms, including anxiety, depression, and connective tissue problems, all of which can contribute to SCAD. These cases suggest a possible connection between the fragile X premutation and a predisposition to SCAD.
References: Am J Med Genet A. 2003 Apr 15;118A(2):127-34. (PMID: 12655493)
Am J Med Genet A. 2012 Oct;158A(10):2473-81. (PMID: 22903889)
FASEB J. 2014 Aug;28(8):3313-24. (PMID: 24732132)
Front Psychiatry. 2018 Nov 13;9:564. (PMID: 30483160)
Clin Genet. 2019 Feb;95(2):262-267. (PMID: 30414172)
Circulation. 2018 May 8;137(19):e523-e557. (PMID: 29472380)
Lancet Neurol. 2013 Aug;12(8):786-98. (PMID: 23867198)
Genome Med. 2012 Dec 21;4(12):100. (PMID: 23259642)
J Am Coll Cardiol. 2017 Aug 29;70(9):1148-1158. (PMID: 28838364)
معلومات مُعتمدة: P50 HD103526 United States HD NICHD NIH HHS; R01 HD036071 United States HD NICHD NIH HHS; U54 HD079125 United States HD NICHD NIH HHS; UL1 TR001860 United States TR NCATS NIH HHS
تواريخ الأحداث: Date Created: 20200311 Latest Revision: 20240328
رمز التحديث: 20240329
مُعرف محوري في PubMed: PMC7062363
DOI: 10.1016/j.jaccas.2019.11.058
PMID: 32154514
قاعدة البيانات: MEDLINE
الوصف
تدمد:2666-0849
DOI:10.1016/j.jaccas.2019.11.058