SETX Gene Ataxiaoculomotor Apraxia Type 2 NGS Genetic DNA Test
Introduction to the Test
The SETX Gene Ataxiaoculomotor Apraxia Type 2 NGS Genetic DNA Test is a significant diagnostic tool used to identify genetic mutations associated with ataxia and oculomotor apraxia. This test employs Next-Generation Sequencing (NGS) technology to analyze the SETX gene, which is linked to neurological disorders. Understanding your genetic makeup can provide valuable information for managing and treating these conditions.
What Does the Test Measure?
This test specifically detects mutations in the SETX gene that may lead to ataxiaoculomotor apraxia type 2. By analyzing the DNA sample, healthcare providers can identify genetic predispositions that may affect motor coordination and eye movement.
Who Should Consider This Test?
Individuals with a family history of neurological disorders, particularly those experiencing symptoms such as:
- Loss of coordination
- Difficulty with eye movements
- Muscle weakness
- Speech difficulties
are encouraged to consider this genetic test. Additionally, those who have experienced unexplained neurological symptoms or have a known family history of SETX gene mutations should consult their healthcare provider about this test.
Benefits of Taking the Test
- Early detection of genetic predispositions to neurological disorders.
- Informed decision-making regarding treatment and management options.
- Potential for personalized healthcare strategies.
- Guidance for family planning and genetic counseling.
Understanding Your Results
Results from the SETX Gene Ataxiaoculomotor Apraxia Type 2 NGS Genetic DNA Test will provide insights into the presence of mutations. A genetic counselor will help interpret these results, discussing their implications for your health and potential next steps.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| SETX Gene Ataxiaoculomotor Apraxia Type 2 NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book Your Test Today!
To schedule your SETX Gene Ataxiaoculomotor Apraxia Type 2 NGS Genetic DNA Test, please contact us at +2348077798758. Our team is here to assist you with any questions and guide you through the booking process.
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 and a genetic counseling session to draw a pedigree chart of family members affected with SETX Gene Ataxiaoculomotor Apraxia Type 2 are required.
Specialty: Neurology
Department: Genetics
Method: NGS Technology
Disease Type: Neurological Disorders
