SLC1A3 Gene Episodic Ataxia Type 6 NGS Genetic DNA Test
Introduction
The SLC1A3 Gene Episodic Ataxia Type 6 NGS Genetic DNA Test is a specialized genetic test designed to detect mutations in the SLC1A3 gene, which are associated with episodic ataxia type 6, a neurological disorder characterized by recurrent episodes of loss of coordination and balance. This test plays a vital role in understanding the underlying genetic factors contributing to these symptoms, allowing for informed medical decisions.
What the Test Measures
This genetic test utilizes Next Generation Sequencing (NGS) technology to analyze the SLC1A3 gene. It detects specific mutations that may lead to episodic ataxia type 6, providing insight into the genetic basis of this condition.
Who Should Consider This Test?
Individuals experiencing symptoms such as:
- Unexplained episodes of dizziness or imbalance
- Family history of episodic ataxia or other neurological disorders
- Neurological symptoms without a clear diagnosis
should consider this test. Additionally, individuals with risk factors or a family history of SLC1A3 mutations may benefit from genetic testing.
Benefits of Taking the Test
- Provides clarity on the genetic basis of neurological symptoms.
- Enables personalized treatment plans and management strategies.
- Offers valuable information for family planning and genetic counseling.
- Helps in understanding the risk of recurrence in family members.
Understanding Your Results
Results from the SLC1A3 Gene Episodic Ataxia Type 6 NGS Genetic DNA Test will indicate whether any mutations have been detected. A genetic counselor will assist in interpreting these results and discussing their implications for your health and that of your family.
Test Details
| Test Name | Price (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Booking the Test
To book the SLC1A3 Gene Episodic Ataxia Type 6 NGS Genetic DNA Test, please contact us at +2348110567037. Our team is ready to assist you with the booking process and answer 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 is required, along with a Genetic Counseling session to draw a pedigree chart of family members affected with SLC1A3 Gene Episodic Ataxia Type 6.
Consultation with a Neurologist and a specialist in Genetics is recommended for comprehensive care.
