Sale!

CNTN1 Gene Compton-North Congenital Myopathy Genetic Test

4,400 د.إ

-21%

The CNTN1 gene, associated with Compton-North Congenital Myopathy, plays a crucial role in the development and function of the nervous system. Mutations in this gene can lead to a range of neuromuscular disorders, including Compton-North Congenital Myopathy, which is characterized by muscle weakness and developmental issues from birth. Recognizing the significance of early and accurate diagnosis for effective management and treatment, DNA Labs UAE offers a specialized genetic test targeting the CNTN1 gene.

The test is designed to identify mutations within the CNTN1 gene that could indicate the presence of Compton-North Congenital Myopathy, providing vital information for healthcare providers and affected families. This precise genetic analysis is crucial for confirming the diagnosis, understanding the condition’s progression, and exploring potential treatment options tailored to the individual’s genetic makeup.

Conducted in a state-of-the-art facility, the test is available for a cost of 4400 AED. DNA Labs UAE ensures that the process is handled with the utmost care and professionalism, delivering reliable and timely results. By opting for this genetic test, patients and their families can gain insights into the genetic underpinnings of Compton-North Congenital Myopathy, paving the way for a more informed approach to care and management.

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

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.