Heart and blood vessel disorders, known as cardiovascular diseases, are the leading global cause of illness and death. They vary in severity, making diagnosis tricky due to shared symptoms. Accurate identification is vital for proper treatment, aiding healthcare professionals in effective management and timely intervention for better patient outcomes.
Have an unidentified cardiovascular disease
Have a family history of cardiovascular disease or sudden cardiac death
Are experiencing symptoms (shortness of breath, excessive sweating, heart pain, weakness, fainting or unexplained seizures)
Have a clinical diagnosis of irregular cardiovascular structure or function
Are having high cholesterol, obesity, high blood pressure, or diabetes
Have a hereditary cardiovascular disorder and want to estimate the risk of inheritance to your children
Need cardiovascular surgery and want to predict the right time to undergo this surgery
Panels | No.of genes covered | ||||
---|---|---|---|---|---|
Comprehensive | |||||
Comprehensive Cardiovascular Disorder Panel | 556 | ||||
Comprehensive Congenital Heart Disease | 399 | ||||
Comprehensive Cardiology | 399 | ||||
Individual Panels | |||||
Familial Thoracic Aortic Aneurysm and Dissection | 17 | ||||
Marfan Syndrome | 35 | ||||
Brugada Syndrome | 16 | ||||
Comprehensive Cardiac Arrhythmia | 55 | ||||
Familial Atrial Fibrillation Syndrome | 15 | ||||
Long QT Syndrome | 18 | ||||
Short QT Syndrome | 6 | ||||
Dysplasia | 16 | ||||
Sudden Cardiac Arrest | 49 | ||||
Catecholaminergic Polymorphic Ventricular Tachycardia | 8 | ||||
Dilated Cardiomyopathy | 55 | ||||
Hypertrophic Cardiomyopathy | 50 | ||||
Left Ventricular Noncompaction | 9 | ||||
Pan Cardiomyopathy Panel | 99 | ||||
Alagille Syndrome | 2 | ||||
Nonsyndromic Congenital Heart Disease | 44 | ||||
Noonan Spectrum Disorders | 24 | ||||
Progressive Familial Intrahepatic Cholestasis (PFIC) | 6 | ||||
Disorders of Fatty Acid Oxidation (FAOD) | 33 | ||||
Glutaric Acidemia Type II | 3 | ||||
Ectodermal Dysplasia | 6 | ||||
Ehlers-Danlos Syndromes (EDS) | 64 | ||||
Heterotaxy, Situs Inversus and Kartagener's Syndrome | 45 |