FLNC Gene Filaminopathy Genetic Test
At DNA Labs UAE, we offer the FLNC Gene Filaminopathy Genetic Test to diagnose and identify mutations in the FLNC gene associated with filaminopathy. This rare genetic disorder affects the skeletal muscles, heart, and other organs.
The FLNC gene is responsible for producing proteins that are essential for normal muscle function. Mutations in this gene can disrupt protein production, leading to muscle weakness, joint stiffness, and other symptoms associated with filaminopathy.
We utilize NGS (next-generation sequencing) technology for this genetic test. NGS allows us to analyze multiple genes simultaneously, making it particularly effective for identifying mutations in genes associated with rare diseases like filaminopathy.
To perform the FLNC Gene Filaminopathy Genetic Test, we require a small sample of either blood, extracted DNA, or one drop of blood on an FTA card. These samples will be collected by a neurologist or geneticist.
After sample collection, the test results will be delivered within 3 to 4 weeks. Our laboratory will analyze the sample using NGS technology and provide a comprehensive report to the referring neurologist.
The FLNC Gene Filaminopathy Genetic Test is conducted in our Genetics department, where our experienced team of geneticists and scientists will perform the analysis and interpretation of the test results.
Pre Test Information
Prior to undergoing the FLNC Gene Filaminopathy Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members who may be affected by filaminopathy.
The cost of the FLNC Gene Filaminopathy Genetic Test is AED 4400.0.
This test is typically ordered by a neurologist who suspects filaminopathy based on the patient’s symptoms and clinical history.
The FLNC Gene Filaminopathy Genetic Test offered by DNA Labs UAE is a valuable tool for diagnosing filaminopathy and identifying mutations in the FLNC gene. With our advanced NGS technology and experienced team, we can provide accurate and timely results to help develop a treatment plan for patients.
|FLNC Gene Filaminopathy Genetic Test
|Blood or Extracted DNA or One drop Blood on FTA Card o
|3 to 4 Weeks
|Pre Test Information
|Clinical History of Patient who is going for FLNC Gene Filaminopathy NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with FLNC Gene Filaminopathy
The FLNC gene is associated with a rare genetic disorder called filaminopathy, which affects the skeletal muscles, heart, and other organs. Filaminopathy is caused by mutations in the FLNC gene that lead to abnormal protein production, which in turn causes muscle weakness, joint stiffness, and other symptoms.
NGS (next-generation sequencing) genetic testing is a type of genetic testing that uses advanced technology to analyze multiple genes at once. This type of testing is particularly useful for identifying mutations in genes like FLNC that are associated with rare diseases.
FLNC gene filaminopathy NGS genetic testing involves collecting a small sample of blood or saliva from the patient and analyzing it in a laboratory. The test can detect mutations in the FLNC gene and other genes associated with filaminopathy. The results of the test can help doctors diagnose filaminopathy and develop a treatment plan for the patient.