Anomalous Coronary Artery Origin in a Young Patient with Marfan Syndrome
Joint Authors
César, Luiz Antonio Machado
Duarte, S. B. C. P.
Beraldo, D. O.
Takada, Julio Yoshio
Mansur, Antonio de Padua
Source
Issue
Vol. 2017, Issue 2017 (31 Dec. 2017), pp.1-5, 5 p.
Publisher
Hindawi Publishing Corporation
Publication Date
2017-12-21
Country of Publication
Egypt
No. of Pages
5
Main Subjects
Abstract EN
Marfan syndrome is an autosomal dominant genetic disorder that affects connective tissue and is caused by mutations in the fibrillin 1 gene present at chromosome 15.
Aortic aneurysm is its main complication, and along the dilation of the aorta root and its descending portion (60–100%), with secondary aortic insufficiency, it increases risk of acute aortic dissection and death.
Coronary artery anomalies affect between 0.3% and 1.6% of the general population and are the second leading cause of sudden death in young adults, especially if the anomalous coronary passes through aorta and pulmonary artery.
The anomalous origin of the left main coronary artery in the right Valsalva sinus has a prevalence of 0.02%–0.05% and is commonly related to other congenital cardiac anomalies, such as transposition of great vessels, coronary fistulas, bicuspid aortic valve, and tetralogy of Fallot.
Its association with Marfan syndrome is not known, and there is no previous report in the literature.
We describe here a case of a female with Marfan syndrome diagnosed with symptomatic anomalous origin of the left coronary artery in the right Valsalva sinus.
American Psychological Association (APA)
Duarte, S. B. C. P.& Beraldo, D. O.& César, Luiz Antonio Machado& Mansur, Antonio de Padua& Takada, Julio Yoshio. 2017. Anomalous Coronary Artery Origin in a Young Patient with Marfan Syndrome. Case Reports in Cardiology،Vol. 2017, no. 2017, pp.1-5.
https://search.emarefa.net/detail/BIM-1144022
Modern Language Association (MLA)
Duarte, S. B. C. P.…[et al.]. Anomalous Coronary Artery Origin in a Young Patient with Marfan Syndrome. Case Reports in Cardiology No. 2017 (2017), pp.1-5.
https://search.emarefa.net/detail/BIM-1144022
American Medical Association (AMA)
Duarte, S. B. C. P.& Beraldo, D. O.& César, Luiz Antonio Machado& Mansur, Antonio de Padua& Takada, Julio Yoshio. Anomalous Coronary Artery Origin in a Young Patient with Marfan Syndrome. Case Reports in Cardiology. 2017. Vol. 2017, no. 2017, pp.1-5.
https://search.emarefa.net/detail/BIM-1144022
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references
Record ID
BIM-1144022