ROBO3 Gene Gaze Palsy Horizontal With Progressive Scoliosis NGS Genetic DNA Test
The ROBO3 Gene Gaze Palsy Horizontal with Progressive Scoliosis NGS Genetic DNA Test is a specialized genetic examination aimed at detecting mutations in the ROBO3 gene, which is linked to specific neurological disorders. This test is crucial for understanding genetic predispositions to conditions such as gaze palsy and progressive scoliosis, enabling timely intervention and informed decision-making for affected individuals.
What the Test Measures/Detects
This genetic test utilizes Next-Generation Sequencing (NGS) technology to analyze the ROBO3 gene. It identifies potential mutations that may contribute to neurological disorders, specifically those presenting with gaze palsy and progressive scoliosis.
Who Should Consider This Test?
Individuals exhibiting symptoms such as:
- Gaze palsy
- Progressive scoliosis
- Family history of neurological disorders
Additionally, patients with risk factors for genetic conditions related to the ROBO3 gene should consider this test.
Benefits of Taking the Test
- Provides clarity on genetic predispositions to neurological disorders.
- Facilitates informed healthcare decisions for patients and their families.
- Helps in planning preventive measures or early interventions.
- Guides personalized treatment options based on genetic findings.
Understanding Your Results
Results from the ROBO3 Gene Gaze Palsy Horizontal with Progressive Scoliosis NGS Genetic DNA Test will be provided in a comprehensive report. It is essential to discuss these results with a healthcare provider, particularly a neurologist or genetic counselor, to understand their implications fully.
Test Pricing
| Discount Price | Regular Price |
|---|---|
| 400000 NGN | 560000 NGN |
Booking the Test
To book the ROBO3 Gene Gaze Palsy Horizontal with Progressive Scoliosis NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with scheduling and any inquiries you may have.
Turnaround time for results is approximately 3 to 4 weeks, and the sample type required is either blood, extracted DNA, or one drop of blood on an FTA card. Prior to the test, a clinical history of the patient is necessary, along with a genetic counseling session to draw a pedigree chart of affected family members.
Take the first step towards understanding your genetic health today!
