What is CardioGenomX?
CardioGenomX is a test used to determine genetic predisposition to cardiovascular diseases. This test is recommended for a wide range of individuals, including those who have experienced early-onset vascular occlusion, have family members with a history of heart attack or stroke, exhibit symptoms of hypertension, or have experienced preeclampsia in early pregnancy, among others. Based on the test results, an individual's risk profile for cardiovascular diseases is identified, enabling appropriate measures to be taken for prevention or management of the condition. This contributes to the prevention or mitigation of the progression of the disease.
CardioGenomX is a test panel used to determine genetic predisposition to cardiovascular diseases.
Who is recommended for CardioGenomX?
CardioGenomX is recommended for those who have experienced early-onset vascular occlusion, those with family members who have had heart attacks, strokes, or paralysis, those with low folate levels or high homocysteine or hs-CRP test results in routine screening tests, those with hypertension complaints, those with varicose veins in their legs, those with a history of recurrent miscarriages or stillbirths, those experiencing preeclampsia or developmental difficulties in early pregnancy.
What are the benefits of CardioGenomX?
The CardioGenomX test determines an individual's predisposition to cardiovascular diseases through the analysis of genetic polymorphisms. Thus, it enables appropriate preventive measures to be taken in a timely and accurate manner. Based on the test results, the individual's risk profile is determined, and appropriate treatment or measures can be planned, thereby helping to prevent or mitigate the progression of cardiovascular diseases.
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