TSEN2 Gene Pontocerebellar Hypoplasia Type 2B NGS Genetic DNA Test
Introduction
The TSEN2 Gene Pontocerebellar Hypoplasia Type 2B NGS Genetic DNA Test is a specialized diagnostic tool designed to identify mutations in the TSEN2 gene, which are associated with Pontocerebellar Hypoplasia (PCH) type 2B. This genetic condition primarily affects the development of the brain, particularly the cerebellum and pons, leading to various neurological disorders. Early diagnosis through this test can significantly impact treatment options and outcomes for affected individuals.
What the Test Measures
This genetic test detects specific mutations in the TSEN2 gene using Next Generation Sequencing (NGS) technology. By analyzing the genetic material, healthcare providers can confirm or rule out the presence of genetic abnormalities linked to PCH type 2B.
Who Should Consider This Test
This test is recommended for individuals exhibiting symptoms of neurological disorders, particularly those with developmental delays, motor dysfunction, or intellectual disabilities. Family members of affected individuals may also benefit from testing to understand their genetic risk.
Benefits of Taking the Test
- Accurate diagnosis of TSEN2 gene mutations.
- Informed decision-making regarding treatment and management.
- Guidance for family planning and risk assessment.
- Access to specialized care and resources.
Understanding Your Results
Results from the TSEN2 Gene Pontocerebellar Hypoplasia Type 2B NGS Genetic DNA Test will be interpreted by a qualified genetic counselor or neurologist. They will explain the implications of the findings and discuss potential next steps based on the results.
Test Details and Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| TSEN2 Gene Pontocerebellar Hypoplasia Type 2B NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking Your Test
To book the TSEN2 Gene Pontocerebellar Hypoplasia Type 2B NGS Genetic DNA Test, please contact us at +2348077798758 or visit our website to schedule an appointment. Our team is ready to assist you through the process and provide the necessary guidance for your genetic testing needs.
Additional Information
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One Drop Blood on FTA Card
Pre-Test Instructions: A clinical history of the patient going for the test and a genetic counseling session to draw a pedigree chart of family members affected with TSEN2 Gene Pontocerebellar Hypoplasia Type 2B.
For further inquiries, please reach out to our support team. We are dedicated to providing you with the best diagnostic services in Nigeria.
