Aneurysm risk Panel
Aneurysm risk Panel
Genetic predisposition can increase the risk of the onset of aneurysms, abnormal dilations of the arterial walls, which can cause their rupture. There are, for example, familial forms of aortic aneurysm and dissection, which tend to recur within the same family and which therefore predispose its members. Similarly, one's personal risk of suffering this type of pathological condition can derive from the presence of broader syndromes which, among the various possible pathological manifestations, can also lead to greater fragility of the vascular walls (e.g. Marfan Syndrome).
This panel is particularly suitable for subjects with predisposing syndromes that strongly increase the risk of aneurysm or who have other risk factors. It is also useful for those who have first-degree relatives who have already suffered this type of pathological manifestation.
The analysis takes into consideration the mutation of germline DNA, it investigates SNP and Indel mutations up to 150 bp.
- Available in less than 24 hours
- Based on Whole Genome Sequencing
- More than 160 genes analyzed
- Investigates SNP and Indel mutations up to 150 bp
List of main conditions:
- Ehlers-Danlos Syndrome
- Marfan Syndrome
- Pseudoxanthoma Elasticum-Like Disorder
- Aortic Aneurysm, Familial Thoracic
What You Get
Wellness ReportSee a report
The Wellness Report clarifies which habits are best suited to your genome, with actionable insights to live a better life.
Scientific Fitness ReportSee a report
The Fitness report gives you actionable advice on training, sports, fitness and physical activity. This will help you develop the right workout for you based on your whole genome.
Nutrigenomics ReportSee a report
Learn about the relationships between food groups and your genes. Using this report, you can create the most effective and personalized diet with a specialist.
Health and PredispositionsSee the report
Learn more about your risk to develop +50 diseases and conditions. Start taking a proactive approach to your health with our actionable insights.
How it works
Using a simple at home blood sample, we can collect the 100% of your DNA and analyze the genetic sequence in our lab.
The sequence is divided into several parts, amplified, grouped in clusters and then sequenced.
This sequencing process reveals the order of nucleotides that make up the original DNA sample.
We then compare the genome with a generic and globally recognized reference DNA sequence.
Simple Blood Sample Collection
Painless, quick at home sample collection. User friendly device with CE-IVD mark and FDA approval.
Simply follow the packaging instructions and send the sample back using the pre-paid returns label.
Genomic Consultation Service
Would you like to speak with a genetic specialist? Book an individual session.
Our extensive network of geneticists will provide you with specialized genetic counseling on the topics that are most relevant for you such as diet and nutrition, fitness, injuries and many more.
Check out the full range of our additional reports, available upon completion of the Genome Test.
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