Familial Mediterranean Fever MEFV Full Gene Analysis
Introduction to Familial Mediterranean Fever MEFV Full Gene Analysis
The Familial Mediterranean Fever (FMF) MEFV Full Gene Analysis is a vital genetic test designed to identify mutations in the MEFV gene, which are responsible for FMF, a hereditary inflammatory disorder. This test is crucial for individuals who exhibit symptoms of FMF or have a family history of the condition. Understanding your genetic predisposition can significantly impact your health management and treatment options.
What the Test Measures
This test detects mutations in the MEFV gene, which plays a key role in regulating inflammation in the body. By identifying specific genetic variations, healthcare providers can diagnose FMF and tailor treatment plans accordingly.
Who Should Consider This Test?
Individuals who should consider the Familial Mediterranean Fever MEFV Full Gene Analysis include:
- People with recurrent fevers and abdominal pain.
- Those with a family history of FMF.
- Individuals of Mediterranean descent, where FMF is more common.
Benefits of Taking the Test
Taking the Familial Mediterranean Fever MEFV Full Gene Analysis offers several benefits:
- Accurate diagnosis of FMF, leading to timely treatment.
- Informed decisions regarding family planning and genetic counseling.
- Personalized treatment plans to manage symptoms effectively.
Understanding Your Results
After the test, results will indicate whether mutations are present in the MEFV gene. A genetic counselor or healthcare provider will help interpret these results, guiding you on the next steps for treatment and management of FMF.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 720000 NGN |
| Regular Price | 960000 NGN |
Booking the Test
To book your Familial Mediterranean Fever MEFV Full Gene Analysis, please contact us at +2348077798758 or visit our website. Remember, a doctor’s prescription is required for this test, except for surgery and pregnancy cases or individuals planning to travel abroad.
Additional Information
- Turnaround Time: 4-6 weeks
- Sample Type: Peripheral blood
- Test Components: EDTA Vacutainer (3 ml)
- Method: NGS (Next Generation Sequencing)
- Specialty: General Physician
