DNA tests for detection/prediction of congenital and acquired cardiovascular diseases Prediction of the risks of having cardiovascular disease is a hot area in prevention medicine. The test evaluates the risk of developing a specific disease.
This improves the chance of early diagnosis and treatment of a potential lethal heart disease.
Methods of Examination
遺傳心血管疾病15基因檢查 優點 :
- Screening for 15 commonly involved genes
- Indicated for those with family history of heart disease
- Improved accuracy in the risk prediction of cardiovascular disease
- 有效針對 :
- Indicated for those with family history of heart diseases
- Risk prediction for cardiovascular disease
遺傳心血管疾病76基因檢查優點 :
- Screening for 76 commonly involved genes
- More comprehensive coverage of various heart diseases
- Indicated for those with family history of heart disease
- Improved accuracy in the risk prediction of cardiovascular disease
- 有效針對 :
- Dilated Cadiomyopathies
- Hypertrophic Cardiomyopathies
- Barth Syndrome
- Long QT Syndrome
- Noonan Syndrome
- Fabry’s Disease
- Catecholaminergic Polymorphic Ventricular Tachycardia
- Familial Amyloid Polyneuropathy
- Lysosomal Storage Disorders
- Costello Syndrome
- Duchenne Muscular Dystrophy
- Non-compaction of the Ventricular Myocardium
- Arrhythmogenic Right Ventricular Cardiomyopathy
Who are suitable for DNA tests
- Family history of cardiovascular disease
- Suffering from specific heart disease related to genetic mutation
- History of smoking or alcohol drinking
- Lack of exercise
- Unhealthy dietary habit
- As part of the health risk management program
- History of unexplained syncope or ventricular arrhythmias
- Heavy work stress and lack of quality sleep