First reported case of arrhythmogenic right ventricular cardiomyopathy in Oman
Joint Authors
al-Lawati, Hatim
al-Dhuhli, Hammud
Source
Issue
Vol. 32, Issue 4 (31 Jul. 2017), pp.339-343, 5 p.
Publisher
Publication Date
2017-07-31
Country of Publication
Oman
No. of Pages
5
Main Subjects
Abstract EN
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a rare genetic disorder characterized by fatty degeneration of the right ventricular myocardium with variable involvement of the left ventricle.
The condition is associated with exercise-mediated ventricular tachycardia and is one of the recognized causes of sudden cardiac death in the young and in athletes.
Here, we report the first confirmed case of ARVC in Oman and present its electrocardiographic, echocardiographic features, and radiological findings on gated, contrast-enhanced cardiac computed tomography.
Our patient was a 22-year-old male who had presented to our hospital for evaluation and investigation of syncope and symptomatic palpitations
American Psychological Association (APA)
al-Lawati, Hatim& al-Dhuhli, Hammud. 2017. First reported case of arrhythmogenic right ventricular cardiomyopathy in Oman. Oman Medical Journal،Vol. 32, no. 4, pp.339-343.
https://search.emarefa.net/detail/BIM-748714
Modern Language Association (MLA)
al-Lawati, Hatim& al-Dhuhli, Hammud. First reported case of arrhythmogenic right ventricular cardiomyopathy in Oman. Oman Medical Journal Vol. 32, no. 4 (Jul. 2017), pp.339-343.
https://search.emarefa.net/detail/BIM-748714
American Medical Association (AMA)
al-Lawati, Hatim& al-Dhuhli, Hammud. First reported case of arrhythmogenic right ventricular cardiomyopathy in Oman. Oman Medical Journal. 2017. Vol. 32, no. 4, pp.339-343.
https://search.emarefa.net/detail/BIM-748714
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references : p. 343
Record ID
BIM-748714