TTBK2 Gene Spinocerebellar Ataxia Type 11 Autosomal Dominant NGS Genetic DNA Test
Introduction
The TTBK2 Gene Spinocerebellar Ataxia Type 11 Autosomal Dominant NGS Genetic DNA Test is a vital diagnostic tool that helps identify genetic predispositions to neurological disorders. This test leverages Next Generation Sequencing (NGS) technology to analyze the TTBK2 gene, which is associated with spinocerebellar ataxia type 11, a condition characterized by progressive loss of coordination and balance.
What the Test Measures
This genetic test detects mutations in the TTBK2 gene that may lead to spinocerebellar ataxia type 11. By identifying these mutations, healthcare providers can better understand the risk of developing this disorder and tailor management strategies accordingly.
Who Should Consider This Test
Individuals who exhibit symptoms such as:
- Progressive loss of coordination
- Difficulty with balance
- Slurred speech
- Family history of spinocerebellar ataxia
should consider undergoing this test. Additionally, those with risk factors or a clinical history suggestive of neurological disorders may benefit from testing.
Benefits of Taking the Test
- Early diagnosis and intervention
- Informed family planning and genetic counseling
- Personalized treatment options
- Peace of mind through understanding genetic risks
Understanding Your Results
Results from the TTBK2 Gene Spinocerebellar Ataxia Type 11 test can indicate the presence of mutations linked to the condition. A genetic counseling session is recommended to interpret these results, discuss implications, and explore next steps for management or treatment.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Book the Test
To book the TTBK2 Gene Spinocerebellar Ataxia Type 11 Autosomal Dominant NGS Genetic DNA Test, please contact us at +2348077798758 or visit our website for more information. Your health is our priority, and we are here to assist you every step of the way.
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 is required, along with a genetic counseling session to draw a pedigree chart of family members affected by TTBK2 Gene Spinocerebellar Ataxia Type 11.
This test is essential for anyone concerned about their genetic health and the potential risks associated with neurological disorders. Don’t wait; take control of your health today!
