TTC8 Gene Bardet-Biedl Syndrome Type 8 NGS Genetic DNA Test
Introduction to the Test
The TTC8 Gene Bardet-Biedl Syndrome Type 8 NGS Genetic DNA Test is a specialized genetic test that plays a pivotal role in diagnosing Bardet-Biedl Syndrome (BBS). This syndrome is a rare genetic disorder characterized by a combination of symptoms affecting multiple systems, including vision, kidney function, and obesity. Understanding the genetic underpinnings of BBS is crucial for early intervention and management.
What the Test Measures
This test employs Next Generation Sequencing (NGS) technology to analyze the TTC8 gene, which is associated with Bardet-Biedl Syndrome Type 8. By detecting mutations in this gene, healthcare providers can assess the risk of developing the syndrome and its associated complications.
Who Should Consider This Test?
Individuals who should consider the TTC8 Gene Bardet-Biedl Syndrome Type 8 NGS Genetic DNA Test include:
- Those with a family history of Bardet-Biedl Syndrome.
- Individuals exhibiting symptoms such as obesity, retinal degeneration, and kidney dysfunction.
- Patients with a clinical history suggestive of BBS.
Benefits of Taking the Test
Taking the TTC8 Gene Bardet-Biedl Syndrome Type 8 NGS Genetic DNA Test offers several benefits:
- Early identification of genetic predispositions.
- Informed decision-making regarding health management and family planning.
- Access to targeted treatment options and support services.
Understanding Your Results
Results from the TTC8 Gene Bardet-Biedl Syndrome Type 8 NGS Genetic DNA Test will indicate whether mutations in the TTC8 gene are present. A genetic counseling session is recommended to help interpret the results and discuss potential implications for health and family members.
Test Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| TTC8 Gene Bardet-Biedl Syndrome Type 8 NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking the Test
To book the TTC8 Gene Bardet-Biedl Syndrome Type 8 NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with scheduling and answering any questions you may have.
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 undergoing the test is required, along with a genetic counseling session to draw a pedigree chart of family members affected by Bardet-Biedl Syndrome.
For more information or to schedule your appointment, reach out to us today!
