COL11A1 Gene Marshall Syndrome NGS Genetic DNA Test
Introduction
The COL11A1 Gene Marshall Syndrome NGS Genetic DNA Test is a state-of-the-art diagnostic tool that plays a vital role in understanding genetic disorders linked to the COL11A1 gene. This test employs Next Generation Sequencing (NGS) technology to provide comprehensive insights into the genetic factors contributing to Marshall syndrome, a condition characterized by various ear, nose, and throat disorders.
What the Test Measures
This genetic test specifically measures mutations in the COL11A1 gene, which can lead to developmental abnormalities in connective tissues, affecting the structure and function of the ear, nose, and throat. By identifying these mutations, healthcare providers can make informed decisions regarding diagnosis and treatment.
Who Should Consider This Test
This test is recommended for individuals exhibiting symptoms such as:
- Hearing loss
- Facial dysmorphism
- Joint hypermobility
- Other related ENT disorders
Additionally, individuals with a family history of Marshall syndrome or related genetic disorders should consider this test for early detection and management.
Benefits of Taking the Test
- Early identification of genetic predispositions to Marshall syndrome.
- Informed decision-making regarding treatment options.
- Guidance for family planning and risk assessment.
- Access to tailored management strategies for affected individuals.
Understanding Your Results
Results from the COL11A1 Gene Marshall Syndrome NGS Genetic DNA Test will provide insights into the presence of mutations in the COL11A1 gene. A genetic counselor will assist in interpreting the results, discussing implications for health management and family planning.
Test Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| COL11A1 Gene Marshall Syndrome NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book the Test
To book the COL11A1 Gene Marshall Syndrome NGS Genetic DNA Test or for more information, please contact us at +2348077798758. Our team is ready to assist you with any inquiries and facilitate your testing process.
Additional Information
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-Test Instructions: Clinical history of the patient and a genetic counseling session to draw a pedigree chart of family members affected with PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test.
For more details on how this test can benefit you, don’t hesitate to reach out!
