الملخص
Hypertrophic cardiomyopathy is a genetic disorder in which the interventricular septum is typically more severely hypertrophied compared to other segments of the myocardium. We report a 18-year-old woman who presented in 2024 to a tertiary cardiac care centre in Muscat, Oman, with a history of anterolateral accessory pathway ablation who developed burning chest pain after stress. Transthoracic echocardiography revealed generalised left ventricular hypertrophy with maximal thickness in the infero-lateral wall with mid-cavity obstruction. The symptoms necessitated bisoprolol and disopyramide treatment. As there was an increased risk of sudden cardiac death due to left ventricular wall thickness of more than 30 mm and presence of excessive scarring on magnetic resonance imaging, an implantable cardioverter-defibrillator was placed. Failure of medical therapy led to a myectomy referral. Genetic testing identified a rare Titin gene mutation linked to her cardiomyopathy.
بيانات النشر
- المعرّف الرقمي
- 10.18295/2075-0528.2935
- المجلة
- مجلة جامعة السلطان قابوس الطبية, 25(1), 1076-1080
- الناشر
- جامعة السلطان قابوس
- وصول مفتوح
- وصول مفتوح ذهبي
- الترخيص
- CC BY-ND 4.0
اقتبس هذه المقالة
APA 7
Al-Lawati, K., & Maddali, M. M. (2025). A Rare Titin Gene Mutation Causing Hypertrophic Cardiomyopathy in an Omani Individual. Sultan Qaboos University Medical Journal, 25(1), 1076-1080. https://doi.org/10.18295/2075-0528.2935
MLA 9
Al-Lawati, Kumayl, and Madan M. Maddali. "A Rare Titin Gene Mutation Causing Hypertrophic Cardiomyopathy in an Omani Individual." Sultan Qaboos University Medical Journal, vol. 25, no. 1, 2025, pp. 1076-1080. https://doi.org/10.18295/2075-0528.2935.
شيكاغو (المؤلف–التاريخ)
Al-Lawati, Kumayl, and Madan M. Maddali. 2025. "A Rare Titin Gene Mutation Causing Hypertrophic Cardiomyopathy in an Omani Individual." Sultan Qaboos University Medical Journal 25 (1): 1076-1080. https://doi.org/10.18295/2075-0528.2935.
هارفارد
Al-Lawati, K. and Maddali, M. M. (2025) 'A Rare Titin Gene Mutation Causing Hypertrophic Cardiomyopathy in an Omani Individual', Sultan Qaboos University Medical Journal, 25(1), pp. 1076-1080. doi:10.18295/2075-0528.2935.
فانكوفر
Al-Lawati K, Maddali MM. A Rare Titin Gene Mutation Causing Hypertrophic Cardiomyopathy in an Omani Individual. Sultan Qaboos University Medical Journal. 2025;25(1):1076-1080. doi:10.18295/2075-0528.2935
IEEE
K. Al-Lawati, and M. M. Maddali, "A Rare Titin Gene Mutation Causing Hypertrophic Cardiomyopathy in an Omani Individual," Sultan Qaboos University Medical Journal, vol. 25, no. 1, pp. 1076-1080, 2025, doi: 10.18295/2075-0528.2935.