Sale!

Familial Mediterranean Fever MEFV Full Gene Analysis Test

Original price was: 9,600 د.إ.Current price is: 7,200 د.إ.

-25%

The Familial Mediterranean Fever (FMF) MEFV Full Gene Analysis Test is a comprehensive genetic screening designed to identify mutations in the MEFV gene, which are associated with Familial Mediterranean Fever. This condition is an inherited disorder that primarily affects individuals of Mediterranean and Middle Eastern descent, leading to recurrent fevers and painful inflammation of the abdomen, lungs, and joints. By analyzing the entire MEFV gene, this test can provide crucial information for the diagnosis, management, and treatment planning of FMF.

Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test ensures high accuracy and reliability in results. The cost of the FMF MEFV Full Gene Analysis Test is 7200 AED, reflecting the comprehensive nature of the genetic analysis and the expertise required to interpret its findings. This test is particularly important for individuals with a family history of FMF or those exhibiting symptoms, as early detection can significantly improve the quality of life through targeted treatments and lifestyle adjustments.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
Guaranteed Safe Checkout

Familial Mediterranean Fever MEFV Full Gene Analysis Test

Test Name: Familial Mediterranean Fever MEFV Full Gene Analysis Test

Components: EDTA Vacutainer (3 ml)

Price: 7200.0 AED

Sample Condition: Peripheral blood

Report Delivery: 4-6 weeks

Method: NGS (Next-Generation Sequencing)

Test Type: Genetics

Doctor: General Physician

Test Department: DNA Labs UAE

Pre Test Information

Familial Mediterranean Fever: MEFV full gene analysis can be done with a doctor’s prescription. Please note that the prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.

Test Details

Familial Mediterranean Fever (FMF) is an inherited autoinflammatory disorder that primarily affects people of Mediterranean origin. It is caused by mutations in the MEFV gene, which encodes for a protein called pyrin. Pyrin is involved in regulating the body’s inflammatory response.

There are more than 300 known mutations in the MEFV gene, with the most common mutations found in exons 2, 3, 5, and 10. Genetic testing for FMF typically involves sequencing these exons to identify any mutations. However, a full gene analysis of MEFV involves sequencing the entire gene, including all exons and introns. This comprehensive analysis can identify rare mutations that may not be detected by sequencing only the common exons.

A full gene analysis can also help to identify genetic variants that may contribute to disease severity or treatment response. Various genetic testing methods, such as Sanger sequencing, next-generation sequencing, and targeted gene panels, can be used to perform a full gene analysis of MEFV.

The results of genetic testing can help to confirm a diagnosis of FMF, guide treatment decisions, and provide valuable information for genetic counseling of affected individuals and their families.

Test Name Familial Mediterranean Fever MEFV full gene Analysis Test
Components EDTA Vacutainer (3 ml)
Price 7200.0 AED
Sample Condition Peripheral blood
Report Delivery 4-6 weeks
Method NGS
Test type Genetics
Doctor General Physician
Test Department:
Pre Test Information Familial Mediterranean Fever: MEFV full gene Analysis can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad.
Test Details

Familial Mediterranean Fever (FMF) is an inherited autoinflammatory disorder that primarily affects people of Mediterranean origin. It is caused by mutations in the MEFV gene, which encodes for a protein called pyrin. Pyrin is involved in regulating the body’s inflammatory response.

There are more than 300 known mutations in the MEFV gene, and the most common mutations are found in exons 2, 3, 5, and 10. Genetic testing for FMF typically involves sequencing these exons to identify any mutations.

However, a full gene analysis of MEFV involves sequencing the entire gene, including all exons and introns. This can identify rare mutations that may not be detected by sequencing only the common exons. A full gene analysis can also help to identify genetic variants that may contribute to disease severity or treatment response.

A full gene analysis of MEFV can be performed using a variety of genetic testing methods, including Sanger sequencing, next-generation sequencing, and targeted gene panels. The results of genetic testing can help to confirm a diagnosis of FMF, guide treatment decisions, and inform genetic counseling for affected individuals and their families.