ATP2B3 Gene Spinocerebellar Ataxia Type 1 Xlinked NGS Genetic DNA Test
Introduction
The ATP2B3 Gene Spinocerebellar Ataxia Type 1 Xlinked NGS Genetic DNA Test is a vital diagnostic tool designed to identify genetic mutations associated with Spinocerebellar Ataxia Type 1 (SCA1), a hereditary neurological disorder. This test utilizes Next Generation Sequencing (NGS) technology to analyze the ATP2B3 gene, providing critical insights into an individual’s genetic predisposition to this condition.
What the Test Measures
This genetic test specifically detects mutations in the ATP2B3 gene, which are linked to the development of SCA1. By identifying these mutations, healthcare providers can assess the risk of developing this neurological disorder and offer appropriate management and intervention strategies.
Who Should Consider This Test
Individuals with a family history of Spinocerebellar Ataxia or those experiencing symptoms such as coordination difficulties, balance issues, or unexplained neurological symptoms should consider this test. Risk factors include:
- Family history of SCA1
- Symptoms of ataxia
- Genetic predisposition to neurological disorders
Benefits of Taking the Test
Taking the ATP2B3 Gene Spinocerebellar Ataxia Type 1 Xlinked NGS Genetic DNA Test offers numerous benefits, including:
- Early detection of genetic predisposition to SCA1
- Informed decision-making regarding health management
- Access to genetic counseling and support
- Personalized treatment options based on genetic findings
Understanding Your Results
Results from this test will indicate whether or not mutations in the ATP2B3 gene are present. A positive result may suggest a higher risk of developing SCA1, leading to proactive management strategies. It is essential to discuss results with a healthcare provider for comprehensive understanding and guidance.
Test Details
| Test Name | Discount Price | Regular Price |
|---|---|---|
| ATP2B3 Gene Spinocerebellar Ataxia Type 1 Xlinked NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking the Test
To book the ATP2B3 Gene Spinocerebellar Ataxia Type 1 Xlinked NGS Genetic DNA Test, please contact us at +2348110567037. Our team of experts is ready to assist you with the booking process and any questions you may have.
Additional Information
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-Test Instructions: Clinical History of Patient who is going for ATP2B3 Gene Spinocerebellar Ataxia Type 1, X-linked NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with ATP2B3 Gene Spinocerebellar Ataxia Type 1, X-linked
Consult with a neurologist for further insights and guidance regarding this test.
