Sale!

MEFV Gene Mediterranean Fever Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The MEFV Gene Mediterranean Fever Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the MEFV gene, which is a key indicator for Familial Mediterranean Fever (FMF). FMF is a hereditary inflammatory disorder that primarily affects populations of Mediterranean origin, including but not limited to, Turks, Arabs, Jews, and Armenians. This condition is characterized by recurrent episodes of fever, abdominal pain, chest pain, and arthritis. Early detection through the MEFV gene test is crucial for the effective management and treatment of the condition.

DNA Labs UAE offers this cutting-edge genetic test to identify mutations in the MEFV gene, providing essential information for the diagnosis and treatment planning of Familial Mediterranean Fever. The test is priced at 4400 AED, reflecting the sophisticated technology and expertise required to accurately analyze and interpret the genetic data. Conducted in a state-of-the-art laboratory setting by skilled professionals, this test is a valuable tool for individuals with a family history of FMF or those exhibiting symptoms, enabling timely and appropriate medical interventions.

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

MEFV Gene Mediterranean Fever Genetic Test

Introduction

The MEFV gene, also known as the Mediterranean fever gene, is responsible for producing a protein called pyrin. Mutations in this gene can lead to a condition known as familial Mediterranean fever (FMF), which is characterized by recurrent episodes of fever, abdominal pain, chest pain, and joint inflammation.

Test Components

  • Price: 4400.0 AED
  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
  • Report Delivery: 3 to 4 Weeks
  • Method: NGS Technology
  • Test Type: Metabolic Disorders
  • Doctor: General Physician
  • Test Department: Genetics

Pre Test Information

Prior to undergoing the MEFV gene Mediterranean fever NGS genetic DNA test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected with Mediterranean fever.

Test Details

NGS (Next-Generation Sequencing) is a genetic testing method that allows for the simultaneous analysis of multiple genes, including the MEFV gene. NGS can identify specific mutations or variants in the MEFV gene that are associated with FMF. By performing an NGS genetic test for the MEFV gene, healthcare providers can confirm a diagnosis of FMF and provide appropriate treatment and management strategies for affected individuals. This test can also be used for carrier testing in individuals with a family history of FMF.

It’s important to note that genetic testing for the MEFV gene should be done under the guidance of a healthcare professional or genetic counselor, as they can help interpret the results and provide appropriate counseling and support.

Test Name MEFV Gene Mediterranean fever Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Metabolic Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for MEFV Gene Mediterranean fever NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Mediterranean fever
Test Details

The MEFV gene, also known as the Mediterranean fever gene, is responsible for producing a protein called pyrin. Mutations in this gene can lead to a condition known as familial Mediterranean fever (FMF), which is characterized by recurrent episodes of fever, abdominal pain, chest pain, and joint inflammation.

NGS (Next-Generation Sequencing) is a genetic testing method that allows for the simultaneous analysis of multiple genes, including the MEFV gene. NGS can identify specific mutations or variants in the MEFV gene that are associated with FMF.

By performing an NGS genetic test for the MEFV gene, healthcare providers can confirm a diagnosis of FMF and provide appropriate treatment and management strategies for affected individuals. This test can also be used for carrier testing in individuals with a family history of FMF.

It’s important to note that genetic testing for the MEFV gene should be done under the guidance of a healthcare professional or genetic counselor, as they can help interpret the results and provide appropriate counseling and support.