Abstract
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.
| Original language | English |
|---|---|
| Pages (from-to) | 339-343 |
| Number of pages | 5 |
| Journal | Oman Medical Journal |
| Volume | 32 |
| Issue number | 4 |
| DOIs | |
| Publication status | Published - Jul 1 2017 |
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Keywords
- Arrhythmogenic right ventricular dysplasia
- Tachycardia, ventricular
ASJC Scopus subject areas
- Medicine(all)
Cite this
First reported case of arrhythmogenic right ventricular cardiomyopathy in Oman. / Al Lawati, Hatim; Al Dhuhli, Humoud.
In: Oman Medical Journal, Vol. 32, No. 4, 01.07.2017, p. 339-343.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - First reported case of arrhythmogenic right ventricular cardiomyopathy in Oman
AU - Al Lawati, Hatim
AU - Al Dhuhli, Humoud
PY - 2017/7/1
Y1 - 2017/7/1
N2 - 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.
AB - 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.
KW - Arrhythmogenic right ventricular dysplasia
KW - Tachycardia, ventricular
UR - http://www.scopus.com/inward/record.url?scp=85026896971&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85026896971&partnerID=8YFLogxK
U2 - 10.5001/omj.2017.64
DO - 10.5001/omj.2017.64
M3 - Article
AN - SCOPUS:85026896971
VL - 32
SP - 339
EP - 343
JO - Oman Medical Journal
JF - Oman Medical Journal
SN - 1999-768X
IS - 4
ER -