MTHFR Mutation Analysis Booking | Lahalak Platform
Advanced genetic test revealing your body's ability to process folate, helping identify risks of recurrent clotting and pregnancy complications with high precision.
Scientific name: MTHFR (C677T) Mutation Analysis by PCR
Genetic test using Polymerase Chain Reaction (PCR) to detect the most common mutation (C677T) in the Methylenetetrahydrofolate Reductase (MTHFR) gene. This mutation affects the activity of the enzyme responsible for converting folate to its active form (5-MTHF), which may affect homocysteine metabolism.
Service type
Genetic test (Blood)
Duration
10-15 minutes
Fasting
Fasting is not required
Included Services
- Accurate genetic analysis to detect the C677T mutation in the MTHFR gene using PCR technology.
- Consult a geneticist or a maternal-female health specialist to interpret the results.
- Personal support services from Halak.
Medical Service Information
Conditions & Notices
- Fasting: Not required.
- Sample type: Venous blood sample drawn into an EDTA tube (purple tube) to preserve DNA.
- Consultation: The importance of genetic consultation before and after testing is emphasized in order to understand the implications of the results and the limited risks.
- Consent: Genetic testing requires the patient's understanding and consent to undergo it.
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