Cardio Panel

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A Cardio Plus Blood Test Panel includes Cholesterol (Lipid) Profile, Comprehensive Metabolic Panel (CMP-14) and Complete Blood Count (CBC) with differential and platelets.

Types of Cardio Panels

Aorta Panel - a 53 gene panel that includes assessment of non-coding variants and is ideal for patients who have isolated or syndromic aortic disease presenting with ascending aortic dilatation, aneurysm or dissection.

Arrhythmia Panel - Is indicated when there is a problem with the rate and the rhythm of your heartbeat. For example, your heart can beat too quickly, too slow or with irregular rhythm.

Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) Panel - a form of heart disease that forms in adulthood which is when the right ventricular of the heart is replaced by fat because it’s a disorder of the myocardium

Atrial Fibrillation Panel - a 19 gene panel that includes non-coding variants, which is mainly ideal for patient with the suspicion of a hereditary form of atrial fibrillation.

Brugada Syndrome Panel - a 7 gene panel that includes non-coding variants which is ideal for patients with the suspicion or diagnosis of brugada syndrome.

Cardiomyopathy Panel Updated - a 217 gene panel that includes non-coding variants, in addition it also includes the maternally inherited mitochondrial genome.

Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) Panel. - 9 genes associated with (CPVT) for patients with personal and family history of (CPVT)

Comprehensive Cardiology Panel - a 260 gene panel that includes non-coding variants, it also includes the maternally inherited mitochondrial genome. This panel covers known genetic causes of channelopathies and cardiomyopathies.

Congenital Structural Heart Disease Panel - a 125 gene panel that includes non-coding variants, which is ideal for patients with congenital structural heart disease.

Dilated Cardiomyopathy (DCM) Panel - can be used to confirm a clinical diagnosis of dilated cardiomyopathy or identify at risk individuals. Characterized by enlargement of left ventricle, systolic dysfunction and reduction of hearts contractile force over time.

Ehlers-Danlos Syndrome Panel - 21 genes associated with Ehlers-Danlos Syndrome, typically for patient with a personal and or family history suggestive of (EDS)

Hereditary Hemorrhagic Telangiectasia (HHT) Panel - also known as Osler-Weber-Rendu syndrome, which is a autosomal dominant vascular dysplasia characterized by the presence of arteriovenous malformations of the skin, mucosa and viscera.

Heterotaxy and Situs Inversus Panel - a 34 gene panel that includes non-coding variants, ideal for patients diagnosed with lateral disorder.

Hyperlipidemia Core Panel - a 4 gene panel that includes assessment of non-coding variants which is ideal for patients with clinical suspicion of familial hypercholesterolemia.

Hyperlipidemia Panel - a 18 gene panel that includes non-coding variants which is usually ideal for patients with clinical suspicion or inherited dyslipidemia including familial hypercholesterolemia due to LDL receptors mutation or ligand defective apoB, any type of hypertriglyceridemia and sitosterolemia

Hypertrophic Cardiomyopathy (HCM) Panel - 23 Genes disease where the heart muscles become abnormally thick or swollen.

Left Ventricular Non-Compaction Cardiomyopathy (LVNC) Panel - a 33 gene panel that includes non-coding variants which is ideal for patients with clinical suspicion of left ventricular non compaction cardiomyopathy.

Liddle Syndrome Panel - Is a 2 gene panel that includes assessment of non-coding variants. Is ideal for patients with a clinical suspicion of Liddle Syndrome

Long QT Syndrome (LQTS) Panel - Is a 18 gene panel that includes assessment of non-coding variants. Is ideal for patients with a clinical suspicion or diagnosis of long QT syndrome.

Marfan Syndrome Panel - designed as a genetic diagnostic tool for patients with clinical features of Marfan syndrome. The two major features of Marfan syndrome are vision problems caused by a dislocated lens (ectopia lentis) in one or both eyes and arterial aneurysms and dissection involving especially aorta.

Noonan Syndrome Panel - comprehensive analysis of 18 genes associated with Noonan syndrome and related disorders.

Pulmonary Artery Hypertension (PAH) Panel - 23 gene panel that includes assessment of non-coding variants. Is ideal for patients with a clinical diagnosis of idiopathic or familial pulmonary arterial hypertension

Short QT Syndrome (SQTS) Panel - Is a 5 gene panel that includes assessment of non-coding variants. Is ideal for patients with a clinical suspicion of short QT syndrome (SQTS).

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