AFG3L2 Gene Spastic Ataxia Type 5 Autosomal Recessive NGS Genetic DNA Test
Introduction
The AFG3L2 Gene Spastic Ataxia Type 5 Autosomal Recessive NGS Genetic DNA Test is a specialized diagnostic tool designed to identify genetic mutations associated with spastic ataxia type 5, a rare neurological disorder. This test employs Next-Generation Sequencing (NGS) technology to provide accurate and comprehensive results, enabling healthcare providers to make informed decisions regarding patient management and treatment.
What the Test Measures
This test measures specific mutations in the AFG3L2 gene that are known to cause spastic ataxia type 5. By analyzing the genetic makeup, it helps in understanding whether an individual carries the genetic markers associated with this condition.
Who Should Consider This Test
Individuals with a family history of neurological disorders, particularly those exhibiting symptoms such as:
- Loss of coordination and balance
- Muscle weakness
- Difficulty walking or standing
- Speech difficulties
should consider undergoing this genetic test. Additionally, those who have been advised by a neurologist or have undergone genetic counseling may also benefit from this test.
Benefits of Taking the Test
- Early diagnosis of potential neurological disorders
- Informed family planning and genetic counseling
- Personalized treatment options based on genetic findings
- Peace of mind for patients and their families
Understanding Your Results
Results from the AFG3L2 Gene Spastic Ataxia Type 5 test will provide insights into whether genetic mutations are present. A genetic counselor will help you understand the implications of your results, including possible health risks and recommended next steps.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Booking the Test
To book the AFG3L2 Gene Spastic Ataxia Type 5 Autosomal Recessive NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with any questions and guide you through the booking process.
Ensure you have a clinical history available, and consider scheduling a genetic counseling session to discuss your family’s health background before taking the test.
