SLC6A5 Gene Hyperekplexia NGS Genetic DNA Test
Introduction
The SLC6A5 Gene Hyperekplexia NGS Genetic DNA Test is a specialized genetic test designed to identify mutations in the SLC6A5 gene, which are linked to hyperekplexia, a neurological disorder characterized by exaggerated startle responses. This test is essential for individuals who exhibit symptoms of hyperekplexia or have a family history of the condition, enabling timely diagnosis and appropriate management.
What the Test Measures
This test employs Next Generation Sequencing (NGS) technology to examine the SLC6A5 gene for specific mutations. By detecting these mutations, healthcare providers can better understand the genetic basis of hyperekplexia in affected individuals.
Who Should Consider This Test?
Individuals who should consider the SLC6A5 Gene Hyperekplexia NGS Genetic DNA Test include:
- Patients exhibiting symptoms of hyperekplexia such as excessive startle reactions.
- Individuals with a family history of hyperekplexia or related neurological disorders.
- Patients seeking genetic counseling for family planning or management of symptoms.
Benefits of Taking the Test
Taking the SLC6A5 Gene Hyperekplexia NGS Genetic DNA Test offers several benefits:
- Accurate diagnosis of hyperekplexia, leading to better management strategies.
- Informed family planning decisions based on genetic risk assessments.
- Access to tailored treatment options that can improve quality of life.
Understanding Your Results
Once the test is completed, results will be provided to your healthcare provider, who will help interpret the findings. Understanding the genetic basis of your condition can empower you and your family to make informed decisions regarding treatment and lifestyle adjustments.
Test Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| SLC6A5 Gene Hyperekplexia NGS Genetic DNA Test | 400,000 | 560,000 |
Book the Test
To book the SLC6A5 Gene Hyperekplexia NGS Genetic DNA Test, or for more information, please contact us at +2348077798758. Our team is ready to assist you!
Additional Information
Turnaround time for test results is approximately 3 to 4 weeks. The sample type required can be blood, extracted DNA, or one drop of blood on an FTA card. Prior to the test, a genetic counseling session is recommended to discuss the clinical history and draw a pedigree chart of affected family members.
Specialty: Neurology | Department: Genetics | Method: NGS Technology | Disease Type: Neurological Disorders
