PDYN Gene Spinocerebellar Ataxia Type 23 Autosomal Dominant NGS Genetic DNA Test
Introduction to the Test
The PDYN Gene Spinocerebellar Ataxia Type 23 Autosomal Dominant NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify genetic mutations associated with Spinocerebellar Ataxia Type 23 (SCA23). This neurological disorder is characterized by progressive loss of coordination and balance, leading to significant impairment in daily activities. Understanding your genetic predisposition is crucial for effective management and planning.
What the Test Measures
This test utilizes Next-Generation Sequencing (NGS) technology to detect mutations in the PDYN gene, which are linked to the autosomal dominant form of Spinocerebellar Ataxia. By analyzing your DNA, we can identify potential genetic risks and provide personalized insights into your health.
Who Should Consider This Test?
Individuals with a family history of Spinocerebellar Ataxia or those experiencing symptoms such as:
- Loss of coordination
- Difficulty walking
- Speech difficulties
- Hand tremors
should consider this test. Additionally, those with risk factors such as a known family history of the PDYN gene mutation may benefit from early testing.
Benefits of Taking the Test
- Early identification of genetic predisposition to SCA23.
- Informed family planning and management strategies.
- Access to genetic counseling for affected individuals and families.
- Peace of mind through understanding your genetic health.
Understanding Your Results
Results from the PDYN Gene Spinocerebellar Ataxia Type 23 test will provide insights into whether you carry the gene mutation associated with this disorder. It is essential to discuss your results with a healthcare professional, preferably a neurologist or genetic counselor, who can guide you through the implications of your findings.
Test Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| PDYN Gene Spinocerebellar Ataxia Type 23 Autosomal Dominant NGS Genetic DNA Test | 400,000 | 560,000 |
Booking Your Test
To book the PDYN Gene Spinocerebellar Ataxia Type 23 Autosomal Dominant NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with any questions and help you schedule your appointment.
Turnaround time for results is approximately 3 to 4 weeks. Sample types accepted include blood, extracted DNA, or one drop of blood on an FTA card. Prior to testing, a genetic counseling session is recommended to discuss your clinical history and draw a pedigree chart of family members affected by SCA23.
Take control of your health today by understanding your genetic risks. Book your test now!
