Hypertrygliceridemia Report
Hypertrygliceridemia
Hypertriglyceridemia is characterized by an increase in triglycerides in the blood. When we talk about Hypertriglyceridemia, we are generally referring to multifactorial forms, in which an incorrect lifestyle plays an essential role in its onset. However, there are also genetic forms, defined as primary, determined by mutations in specific genes coding for transport proteins or enzymes involved in lipid metabolism.
more than 10 genes analyzed
It is recommended if:
This panel is particularly suitable for those who, especially at a young age, have a clinical suspicion of familial hypercholesterolemia.
List of main conditions:
- Hypertriglyceridemia, susceptibility to
- Hypercholesterolemia, familial, 2
- Hypertriglyceridemia 2
Simple workflow
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FAQs
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Your data is yours. Which is why we have developed proprietary software linked to a dedicated platform, the Genome Manager, to provide you with unique access to your data whenever you want, wherever you are.
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You will be provided with a digital version of the raw data and reports. Thanks to these in-depth tools, you will be able to share your preferred information with your geneticist and/or doctor to indicate and plan the healthiest course for you.
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*Raw data will be available free of charge for the first 30 days after release.
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