Purpose of the Procedure
- Identify causes of unexplained recurrent miscarriages
- Assess risk for Deep Vein Thrombosis (DVT)
- Check how the body processes folic acid
- Detect causes of elevated homocysteine levels
Book MTHFR Mutation Test in Saudi Arabia | Lahalak Medical Platform
A precise genetic test to detect MTHFR gene mutations linked to blood clotting and recurrent miscarriages, helping develop a preventive treatment plan to ensure the safety of both mother and baby.
Scientific name: MTHFR Gene Mutation Testing
A laboratory test to detect C677T and A1298C mutations in the MTHFR gene, which processes folic acid, assessing risks for thrombosis and recurrent pregnancy complications to ensure preventive care.
Service type
Genetic laboratory test
Duration
15-20 minutes
Fasting
Fasting is not required
Included Services
- Blood sample collection
- C677T mutation analysis
- A1298C mutation analysis
- Detailed medical report
Medical Service Information
Target Groups
- Women with a history of recurrent pregnancy loss
- Individuals with a family history of gene mutations
- Patients with early-onset blood clots
- Individuals with high homocysteine levels
Preparation
- Fasting is not required for this genetic test
- Stay well-hydrated to facilitate the blood draw
- Disclose all vitamins and supplements to the specialist
Conditions & Notices
- Please inform the doctor of any blood-thinning medications currently being taken
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