KCNMA1 Gene Generalized Epilepsy and Paroxysmal Dyskinesia NGS Genetic DNA Test
Introduction
The KCNMA1 Gene Generalized Epilepsy and Paroxysmal Dyskinesia NGS Genetic DNA Test is a cutting-edge diagnostic tool that employs Next-Generation Sequencing (NGS) technology to analyze genetic variations associated with neurological disorders. This test is crucial for individuals experiencing unexplained seizures or movement disorders, providing valuable insights into the underlying genetic causes.
What the Test Measures
This genetic test specifically assesses the KCNMA1 gene, which plays a significant role in neuronal excitability and muscle contractions. By identifying mutations or variations in this gene, healthcare providers can determine the likelihood of developing generalized epilepsy or paroxysmal dyskinesia.
Who Should Consider This Test?
Individuals who experience:
- Recurrent seizures
- Unexplained movement disorders
- Family history of epilepsy or dyskinesia
should consider this test. Additionally, those with a clinical history suggestive of genetic neurological disorders are encouraged to seek this testing option.
Benefits of Taking the Test
Understanding your genetic predisposition can:
- Guide treatment decisions and management strategies
- Provide clarity for family planning and genetic counseling
- Assist in identifying potential risks for family members
Understanding Your Results
Results from the KCNMA1 Gene test will indicate whether there are any mutations present in the gene. A genetic counseling session is recommended to help interpret the results and discuss potential implications for treatment and family members.
Test Price
| Discount Price | 400000 NGN |
|---|---|
| Regular Price | 560000 NGN |
How to Book the Test
To book the KCNMA1 Gene Generalized Epilepsy and Paroxysmal Dyskinesia NGS Genetic DNA Test, contact us at +2348077798758. Our team is ready to assist you through the booking process and answer any questions you may have.
Turnaround time for results is approximately 3 to 4 weeks, and samples can be collected via blood or extracted DNA.
Ensure you have a clinical history prepared and consider a genetic counseling session to discuss your family’s medical history before undergoing the test.
