Thrombophilia analysis: the MTHFR gene, factor V, factor II and other factors involved in blood coagulation
Hereditary thrombophilia can manifest itself in mild or severe form in the course of life. For this reason, there is an increasing interest in the use of new genetic markers to identify subjects who present a genetic predisposition to develop cardiovascular diseases.
Who is it aimed to?
All suffering from heart disease, subjects with high cholesterol, hypertensive, those who have high levels of homocysteine in the blood and family members of patients with thrombotic events. All women who intend to take or are taking oral contraceptives and women in old age who need replacement estrogen therapy. Women with early multiple abortion stories and all pregnant women who must evaluate the thrombotic risk.
Discover our packages for a complete gynecological check up or for prenatal screening
How is it performed?
All you need to do is book an appointment to take a simple blood sample or a buccal swab at our laboratory. Samples and swabs can be carried out, by appointment, from 9.30am to 4.30pm and there is no need to fast.
The test can be carried out on a self-collected swab which can be carried out externally to the facility (it is possible to request the material to perform the buccal swab from Genechron).
The external sample delivered must be accompanied by a specific form for samples taken externally.
The reporting timing depends on the analysis and will be calculated by the acceptance of the sample.
The Genechron laboratory, thanks to modern molecular biology techniques, provides valid classic tests validated and CE-IVD tests for the analysis of genetic variants affecting genes that prepare thrombophilia.
The tests offered by Genechron include convenient panels of 6 or 15 mutations:
Panel 15 mutation at €140
- Factor V (R506Q o 1691G/A o Leiden)
- Factor V polimorfismo Y1702C
- Fattore V Cambridge
- Fattore V polimorfismo H1299R
- Fattore II – Protrombina (G20210A)
- MTHFR polimorfismo C677T
- MTHFR polimorfismo A1298C
- HPA
- PAI-1
- Factor XIII
- Beta Fibrinogeno
- CBS
- ATR
- ACE
- AGT
Panel 6 mutation at €80
- Factor V (R506Q o 1691G/A o Leiden)
- Factor V polimorfismo H1299R
- Factor V polimorfismo Y1702C
- Factor II – Protrombina (G20210A)
- MTHFR polimorfismo C677T
- MTHFR polimorfismo A1298C
How to book
- by calling 06.5036729
- by sending a WhatsApp text 388.9233366
- by sending an email to prenotazioni@genechron.com with an appointment request
From Research to Advanced Health Care Diagnostics
CONTACT US WITHOUT COMMITMENT WITH THE METHOD YOU PREFER
+39.06.5036729
info@genechron.com
