myCardio

We analyze hereditary cardiovascular disease risk.

What it is

myCardio is a genetic test that analyzes DNA through Whole Exome Sequencing (WES) to learn if pathogenic variants related to inherited cardiovascular disease are present.

Who it is addressed to

Family history involving sudden cardiac death or unexplained syncope
Athletes who suffer from hypertrophic cardiomyopathy and no family history of it
People suffering from arrhythmogenic right ventricular cardiomyopathy
QT interval ECG abnormalities
Echocardiogram abnormalities
Non-secondary myocardial hypertrophy
Primary dilated cardiomyopathy
Aortic dilation
Possible Brugada syndrome
Possible familial heart disease

Process

You request the test at our center
We will send you a kit to collect a sample
Our representative will collect the sample and deliver it to our authorized laboratories, where sequencing and interpretation will be performed.
The patient will have the option to choose to whom the report will be communicated.
The service is complete with a specialist consultation with the patient, to better explain the results and possible implications.

Why choose myCardio

Simple

All that is needed is a sample of saliva or arterial or venous blood.

Accurate

We analyze 100 genes related to the most common cardiovascular diseases

Preventive

For those who are afraid of inheriting cardiovascular disease

Reliable

The genes analyzed were chosen according to a degree of evidence (Moderate, Strong, or Definite) from the gene-disease association

Additional services

After myCardio has been performed, the genetic analysis can be expanded:

Additional genes that you are most interested in
Exome Diagnostic service
Data reanalysis service so patients can benefit continuously from progress in scientific knowledge

in only takes 15 minutes