CNTN1 Gene Compton-North Congenital Myopathy Genetic Test
Welcome to DNA Labs UAE, your trusted genetic testing laboratory in the UAE. Today, we will be discussing the CNTN1 Gene Compton-North Congenital Myopathy Genetic Test, its cost, symptoms, diagnosis, and other important details.
Test Details
The CNTN1 gene is associated with Compton-North congenital myopathy, a rare genetic disorder that affects muscle function. Our laboratory utilizes NGS (next-generation sequencing) technology to analyze the CNTN1 gene for mutations and variations that may be linked to this condition. This highly accurate and comprehensive method of genetic analysis can detect a wide range of genetic variations, helping to diagnose Compton-North congenital myopathy and guide treatment decisions.
Test Name
CNTN1 Gene Compton-North Congenital Myopathy 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: Neurological Disorders
- Doctor: Neurologist
- Test Department: Genetics
Pre Test Information
Prior to undergoing the CNTN1 Gene Compton-North Congenital Myopathy 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 affected with CNTN1 Gene Compton-North Congenital Myopathy. This information is crucial for a comprehensive analysis and accurate diagnosis.
At DNA Labs UAE, we are committed to providing the highest quality genetic testing services. Our team of experts, including neurologists and geneticists, work together to ensure accurate results and personalized treatment recommendations.
Don’t delay, get tested today and gain valuable insights into your genetic health. Contact DNA Labs UAE to schedule an appointment or for more information about the CNTN1 Gene Compton-North Congenital Myopathy Genetic Test.
Test Name | CNTN1 Gene Compton-North congenital myopathy Genetic Test |
---|---|
Components | |
Price | 4400.0 AED |
Sample Condition | Blood or Extracted DNA or One drop Blood on FTA Card o |
Report Delivery | 3 to 4 Weeks |
Method | NGS Technology |
Test type | Neurological Disorders |
Doctor | Neurologist |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for CNTN1 Gene Compton-North congenital myopathy NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with CNTN1 Gene Compton-North congenital myopathy |
Test Details | The CNTN1 gene is associated with Compton-North congenital myopathy, a rare genetic disorder that affects muscle function. NGS (next-generation sequencing) genetic testing can be used to analyze the CNTN1 gene for mutations and variations that may be linked to this condition. This type of testing can help diagnose Compton-North congenital myopathy and guide treatment decisions. It can also provide information about the risk of passing the condition on to future generations. NGS testing is a highly accurate and comprehensive method of genetic analysis that can detect a wide range of genetic variations. |