WASHC5 Gene SPG8 NGS Genetic DNA Test
Introduction
The WASHC5 Gene SPG8 NGS Genetic DNA Test is a sophisticated diagnostic tool designed to assess genetic variations associated with neurological disorders. This test employs Next-Generation Sequencing (NGS) technology to provide a comprehensive analysis of the WASHC5 gene, which plays a critical role in neuronal function and development.
What the Test Measures
This genetic test detects mutations and variations in the WASHC5 gene that may contribute to the development of specific neurological disorders. By identifying these genetic alterations, healthcare providers can better understand the underlying causes of symptoms experienced by patients.
Who Should Consider This Test?
Individuals who have a family history of neurological disorders or those experiencing related symptoms such as:
- Progressive muscle weakness
- Loss of coordination
- Cognitive decline
- Unexplained neurological symptoms
should consider the WASHC5 Gene SPG8 NGS Genetic DNA Test. Consulting with a neurologist or a genetic counselor is recommended to determine the appropriateness of testing.
Benefits of Taking the Test
- Early identification of genetic risks for neurological disorders.
- Informed decision-making regarding treatment and management options.
- Enhanced understanding of family health history.
- Access to tailored support and resources based on genetic findings.
Understanding Your Results
Results from the WASHC5 Gene SPG8 NGS Genetic DNA Test will be interpreted by a qualified healthcare professional. They will guide you through the implications of the findings, including potential risks for you and your family members. It is important to engage in a genetic counseling session to discuss the results in detail.
Test Details
| Test Name | Price (NGN) |
|---|---|
| WASHC5 Gene SPG8 NGS Genetic DNA Test | Discount Price: 400,000 NGN |
| Regular Price: 560,000 NGN |
Booking Your Test
To schedule your WASHC5 Gene SPG8 NGS Genetic DNA Test, please contact us at +2348077798758 to book your appointment today. Our team is ready to assist you with any inquiries and guide you through the testing 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 is required, along with a genetic counseling session to draw a pedigree chart of family members affected by the WASHC5 Gene SPG8.
Specialty: Neurology
Department: Genetics
Method: NGS Technology
Disease Type: Neurological Disorders
