Genetic Mutations: Identifies 24 known mutations in the MEFV gene, which are responsible for the disease. FMF Diagnosis: Helps confirm the diagnosis in individuals showing recurrent symptoms such as fever and abdominal pain. Genetic Risk Assessment: Allows families to understand the likelihood of passing the disease to future generations. Treatment Guidance: Provides information to help doctors develop an appropriate treatment plan based on the detected mutations.

Individuals Showing FMF Symptoms: Such as recurrent fever attacks, severe abdominal pain, and arthritis. People with a Family History: Those with relatives affected by Familial Mediterranean Fever, increasing their risk. Individuals of Mediterranean Descent: Such as Turks, Arabs, Sephardic Jews, or Armenians, as the disease is more common in these populations. Patients Diagnosed with Chronic Inflammatory Diseases: To help determine if symptoms are caused by FMF. Individuals Needing Genetic Assessment: As part of genetic counseling or before pregnancy to understand potential risks.

Recurrent Fever Attacks: Sudden and periodic increases in body temperature. Severe Abdominal Pain: Usually recurrent and may resemble colic. Arthritis: Swelling and pain in the joints, especially knees and ankles. Skin Rash: Such as vasculitic rash that may appear during attacks. Other Inflammatory Symptoms: Such as lung inflammation or soft tissue inflammation. Family History of the Disease: Presence of family members affected by FMF or similar symptoms.

What is the FMF Test? It is a genetic test used to identify mutations associated with Familial Mediterranean Fever. Why is this test performed? To confirm FMF diagnosis when specific symptoms or a family history of the disease are present. How is the test performed? A blood sample is drawn and analyzed in the laboratory for 24 known mutations in the MEFV gene. Does the test require any special preparations? Usually, no preparations are needed, but it is recommended to consult the doctor regarding any medications taken. How long does it take to get results? Results typically appear within one to two weeks, depending on the laboratory. What are the risks associated with the test? Risks are minimal, including discomfort during the blood draw or minor bruising. What do the test results mean? Positive results indicate the presence of mutations associated with FMF, while negative results may require additional evaluations.

Positive Results: Indicate the presence of a specific mutation associated with the disease, meaning the person may be affected or at risk of developing Familial Mediterranean Fever. Negative Results: Mean that no known mutations were detected, but this does not rule out other conditions or unknown mutations.

Comprehensive FMF 24-Mutation Test | Lahalak Platform

An expanded genetic test covering 24 mutations to diagnose Familial Mediterranean Fever with high accuracy, ensuring a proactive treatment plan to protect you and your family.

Prices starts from: 506.87 SAR

Scientific name: Familial Mediterranean Fever (FMF) 24-Mutation Test

The Familial Mediterranean Fever (FMF) 24 Mutation test is a genetic test used to identify mutations associated with FMF, a genetic disorder that causes recurrent episodes of fever and abdominal pain. This test is essential for diagnosing the condition, especially in individuals with a family history or similar symptoms. The test is performed by co...

Familial Mediterranean Fever (FMF) 24-Mutation Test - Comprehensive FMF 24-Mutation Test

Service type Genetic Test (Blood)

Duration 10-15 minutes

Fasting Fasting is not required

Prices Starting from 506.87 SAR

Included Services

Familial Mediterranean Fever - FMF 24-Mutation Test
The optimal health guidance based on the result.
Personal support services from Lahalak

Medical Service Information

Purpose Test

Genetic Mutations: Identifies 24 known mutations in the MEFV gene, which are responsible for the disease.
FMF Diagnosis: Helps confirm the diagnosis in individuals showing recurrent symptoms such as fever and abdominal pain.
Genetic Risk Assessment: Allows families to understand the likelihood of passing the disease to future generations.
Treatment Guidance: Provides information to help doctors develop an appropriate treatment plan based on the detected mutations.

Recommended groups

Individuals Showing FMF Symptoms: Such as recurrent fever attacks, severe abdominal pain, and arthritis.
People with a Family History: Those with relatives affected by Familial Mediterranean Fever, increasing their risk.
Individuals of Mediterranean Descent: Such as Turks, Arabs, Sephardic Jews, or Armenians, as the disease is more common in these populations.
Patients Diagnosed with Chronic Inflammatory Diseases: To help determine if symptoms are caused by FMF.
Individuals Needing Genetic Assessment: As part of genetic counseling or before pregnancy to understand potential risks.

Symptoms indicative

Recurrent Fever Attacks: Sudden and periodic increases in body temperature.
Severe Abdominal Pain: Usually recurrent and may resemble colic.
Arthritis: Swelling and pain in the joints, especially knees and ankles.
Skin Rash: Such as vasculitic rash that may appear during attacks.
Other Inflammatory Symptoms: Such as lung inflammation or soft tissue inflammation.
Family History of the Disease: Presence of family members affected by FMF or similar symptoms.

FAQs

What is the FMF Test? It is a genetic test used to identify mutations associated with Familial Mediterranean Fever.
Why is this test performed? To confirm FMF diagnosis when specific symptoms or a family history of the disease are present.
How is the test performed? A blood sample is drawn and analyzed in the laboratory for 24 known mutations in the MEFV gene.
Does the test require any special preparations? Usually, no preparations are needed, but it is recommended to consult the doctor regarding any medications taken.
How long does it take to get results? Results typically appear within one to two weeks, depending on the laboratory.
What are the risks associated with the test? Risks are minimal, including discomfort during the blood draw or minor bruising.

Normal Levels

Positive Results: Indicate the presence of a specific mutation associated with the disease, meaning the person may be affected or at risk of developing Familial Mediterranean Fever.
Negative Results: Mean that no known mutations were detected, but this does not rule out other conditions or unknown mutations.