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Familial Mediterranean Fever (FMF) is an inherited disorder characterized by recurrent episodes of fever and inflammation in the abdomen, chest, joints, or skin. FMF is caused by mutations in the MEFV gene, which encodes a protein called pyrin. The FMF test is a diagnostic tool offered by ACL Laboratory that can identify mutations in the MEFV gene, enabling clinicians to make an accurate diagnosis and provide prompt treatment.
What is the FMF Test?
The FMF test is a genetic test that identifies mutations in the MEFV gene. The test is performed using a blood sample and can detect the most common mutations associated with FMF. The results of the test can help clinicians make an accurate diagnosis of FMF and provide prompt treatment.
Why use the FMF Test?
The FMF test offered by ACL Laboratory offers several benefits:
1. Accurate: The FMF test is highly accurate and can detect the most common mutations associated with FMF.
2. Early diagnosis: Early diagnosis of FMF is critical for prompt treatment and management of the disease.
3. Avoidance of unnecessary treatments: The FMF test can help avoid unnecessary treatments for patients who do not have FMF, reducing healthcare costs and improving patient outcomes.
4. Informed decision-making: The results of the FMF test can help clinicians make informed decisions about treatment options and genetic counseling.
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