BEAN1 Gene Spinocerebellar Ataxia Type 31 Autosomal Dominant NGS Genetic DNA Test

Understanding Your Neurological Health Concerns

When coordination problems, balance issues, or unexplained movement difficulties affect your daily life, it’s natural to feel concerned and seek answers. The BEAN1 Gene Spinocerebellar Ataxia Type 31 test provides the clarity you need about hereditary neurological conditions that may run in your family. As a progressive disorder that can impact coordination, speech, and movement, early detection through genetic testing offers the opportunity for proactive health management and informed family planning decisions.

What This Test Detects

This advanced genetic test specifically examines the BEAN1 gene for mutations that cause Spinocerebellar Ataxia Type 31, an autosomal dominant condition. Using Next-Generation Sequencing (NGS) technology, we analyse your DNA to identify specific genetic variations that lead to progressive degeneration of the cerebellum – the part of your brain responsible for coordinating movement and maintaining balance. Unlike general neurological screenings, this targeted test provides definitive answers about your genetic predisposition to this specific hereditary condition.

Who Should Consider This Test

This test is particularly important if you’re experiencing:

• Unexplained coordination difficulties or balance problems
• Family history of neurological disorders or movement conditions
• Progressive speech difficulties or swallowing problems
• Concerns about passing hereditary conditions to children
• Early symptoms of ataxia or cerebellar dysfunction
• Planning for pregnancy with family neurological history

Why Early Detection Matters for Your Health

Identifying BEAN1 gene mutations early provides significant advantages for your neurological health journey. Early detection allows for:

• Proactive symptom management and treatment planning
• Informed family planning decisions and genetic counselling
• Access to appropriate neurological care and specialists
• Peace of mind through definitive genetic answers
• Opportunity to participate in clinical trials and research
• Better preparation for potential future health needs

Understanding Your Test Results

Our comprehensive results provide clear, understandable information about your genetic status. You’ll receive:

• Definitive identification of BEAN1 gene mutations if present
• Clear explanation of what your results mean for your health
• Guidance on next steps and specialist referrals if needed
• Information about inheritance patterns and family implications
• Access to genetic counselling for result interpretation
• Support resources for managing your neurological health

Comprehensive Pricing and Value

Nationwide Trust and Accessibility

Oracle Genomics brings expert neurological genetic testing to communities across South Africa. With convenient testing locations in Johannesburg, Cape Town, Durban, and Pretoria, we ensure that quality genetic healthcare is accessible when and where you need it. Our partnership with leading neurologists and genetic specialists guarantees that you receive the highest standard of care and accurate results you can trust.

Take Control of Your Neurological Health Today

Don’t let uncertainty about hereditary neurological conditions create unnecessary anxiety. Our BEAN1 Gene Spinocerebellar Ataxia Type 31 test provides the answers you need to make informed health decisions. With our special pricing of ZAR 6,700 and comprehensive genetic counselling included, there’s never been a better time to take this important step for your health and your family’s future.

Test Details:
Turnaround Time: 3-4 Weeks
Sample Type: Blood, Extracted DNA, or Blood on FTA Card
Method: Advanced NGS Technology
Professional Support: Genetic Counselling Included