…dominant family, whereas heterozygous carriers of an X linked condition may develop a phenotype later and require delayed or individualized assessment. Disease specific genetic architecture…

…failure and arrhythmias. Family History of Sudden Cardiac Death (FHSCD) : A history of SCD in close relatives suggests a genetic predisposition to arrhythmias. Non Sustained…

…people with a family history of premature cardiovascular disease; those with a family history of high Lp(a); individuals with cardiovascular disease that is not…

…in patients with chest pain (chest discomfort) HISTORY PARAMETER QUESTIONS COMMENTS Risk factors for the 5 serious etiologies Family history (focus on ischemic heart disease…

…aorta, aortic arch) All individuals 60 mm (descending aorta) All individuals Risk factors : previous dissection, family history of dissection, severe aortic regurgitation or mitral regurgitation…

…to ECG interpretation 1. Which of the following ECG findings is typically considered a normal variant in asymptomatic athletes with no significant family history? A:…

…idiopathic or genetic dilation of the left ventricle . Patients with DCM typically develop heart failure early in life and a family history of heart failure…

…and alcohol consumption. Additional considerations include psychosocial stress, obstructive sleep apnoea, social determinants of health, air pollution, family history, ethnicity, and frailty. Primary prevention is…

…hypertension, hypercholesterolaemia, and sedentary behaviour; family history, particularly in the broader assessment of peripheral arterial and aortic disease; planned surgery, especially carotid endarterectomy (CEA), coronary…

…Family history also increases risk, particularly among first degree relatives, with siblings appearing to be especially affected. The principal determinant of adverse outcome is aneurysm…

…or bilateral adrenal hyperplasia. A family history is therefore important, particularly in patients with early onset hypertension or premature cerebrovascular disease. PA is associated with…

…syndrome – appeared to be hereditary, since many patients reported a family history of the same symptoms and events. Perhaps the most distinguishing feature was the…

…common genetic cause, followed by mutations in LMNA , MYH7 , and TNNT2 [39] . Consequently, current guidelines recommend a 3 generation family history and consideration of genetic…

…A personal history of premature CAD, cerebral vascular disease or peripheral vascular disease. A family history of premature myocardial infarction, vascular disease or marked hypercholesterolaemia…

…sex Low body mass index Asian ancestry Previous muscle disease or a personal or family history of muscle disorders Acute infection Renal or hepatic impairment…

…reported with systemic sclerosis, Addison disease, SLE and type 1 diabetes. Traditional factors such as smoking, family history of premature coronary disease, hypertension and hypercholesterolaemia…

…population screening test. It may also be considered in selected lower risk individuals with a family history of premature coronary artery disease. CAC findings incidentally…

…cardiac syndrome. The underlying genetic abnormality is yet to be discovered. Diagnosis of this syndrome is based on ECG, family history and clinical presentation. Patients…