CHRNA4 Gene Epilepsy Nocturnal Frontal Lobe Type 1 NGS Genetic DNA Test
Introduction
The CHRNA4 Gene Epilepsy Nocturnal Frontal Lobe Type 1 NGS Genetic DNA Test is a revolutionary diagnostic tool designed to identify genetic predispositions to neurological disorders, specifically those associated with the CHRNA4 gene. This test is essential for individuals with a family history of epilepsy or related conditions, providing insights that can guide treatment and management strategies.
What the Test Measures
This genetic test utilizes Next Generation Sequencing (NGS) technology to analyze the CHRNA4 gene, which plays a crucial role in neuronal function. It detects mutations that may lead to nocturnal frontal lobe epilepsy, enabling healthcare providers to make informed decisions regarding patient care.
Who Should Consider This Test?
Individuals exhibiting symptoms such as:
- Frequent nocturnal seizures
- Abnormal sleep behaviors
- Family history of epilepsy or neurological disorders
- Unexplained neurological symptoms
should consider undergoing this test. Additionally, those at risk due to family lineage or previous diagnoses may benefit significantly from this genetic evaluation.
Benefits of Taking the Test
- Early identification of genetic risks associated with epilepsy.
- Guidance for personalized treatment plans.
- Informed family planning and genetic counseling.
- Peace of mind through understanding genetic health.
Understanding Your Results
Results from the CHRNA4 Gene Epilepsy Nocturnal Frontal Lobe Type 1 NGS Genetic DNA Test will provide insight into the presence of genetic mutations. A genetic counselor will help interpret these results, discussing their implications for your health and potential risks for family members.
Test Pricing
| Discount Price | Regular Price |
|---|---|
| 400,000 NGN | 560,000 NGN |
Book Your Test Today!
Don’t wait to understand your genetic health. Book the CHRNA4 Gene Epilepsy Nocturnal Frontal Lobe Type 1 NGS Genetic DNA Test today! Contact us at +2348077798758 to schedule your appointment or for more information.
Turnaround time for results is approximately 3 to 4 weeks, and the sample type required for this test can be blood or extracted DNA, or even one drop of blood on an FTA card. Ensure to provide a detailed clinical history and consider a genetic counseling session to create a pedigree chart of affected family members prior to testing.
This test is conducted under the supervision of qualified neurologists and genetic specialists, ensuring you receive the highest standard of care and expertise.
