RUBCN Gene Salih Ataxia NGS Genetic DNA Test
Comprehensive Genetic Testing for Hereditary Neurological Disorders
The RUBCN Gene Salih Ataxia NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics, specifically designed to identify mutations in the RUBCN gene responsible for Salih ataxia. This rare hereditary condition affects the nervous system, leading to progressive coordination difficulties and movement disorders. Our advanced testing methodology provides patients and healthcare providers with definitive genetic information crucial for accurate diagnosis and personalized treatment planning.
What Does This Test Measure?
This specialized genetic test utilizes next-generation sequencing (NGS) technology to comprehensively analyze the RUBCN gene for pathogenic variants associated with Salih ataxia. The test specifically detects:
- Point mutations in the RUBCN gene coding regions
- Small insertions and deletions affecting gene function
- Copy number variations impacting gene dosage
- Pathogenic variants linked to autosomal recessive inheritance patterns
Who Should Consider This Test?
This genetic test is recommended for individuals experiencing symptoms suggestive of hereditary ataxia or those with a family history of neurological disorders. Key indications include:
- Progressive difficulty with coordination and balance
- Unsteady gait and frequent stumbling
- Slurred speech and swallowing difficulties
- Family history of similar neurological symptoms
- Consanguineous parentage in families with neurological disorders
- Unexplained progressive neurological deterioration
Clinical Benefits of RUBCN Gene Testing
Undergoing RUBCN gene testing provides numerous clinical advantages for patients and families:
- Accurate Diagnosis: Confirms or rules out Salih ataxia with high precision
- Treatment Guidance: Informs targeted therapeutic approaches and management strategies
- Genetic Counseling: Provides essential information for family planning decisions
- Prognostic Information: Helps predict disease progression and potential complications
- Family Screening: Enables testing of at-risk family members for early intervention
Understanding Your Test Results
Our comprehensive genetic counseling support helps you interpret your RUBCN gene test results:
- Positive Result: Indicates the presence of pathogenic RUBCN gene mutations associated with Salih ataxia. This confirms the diagnosis and enables appropriate medical management.
- Negative Result: Suggests that RUBCN gene mutations were not detected, though other genetic causes of ataxia may need consideration.
- Variant of Uncertain Significance: Some genetic changes may require additional family studies for proper interpretation.
Test Pricing and Availability
| Test Name | Discount Price | Regular Price |
|---|---|---|
| RUBCN Gene Salih Ataxia NGS Genetic DNA Test | $500 USD | $700 USD |
Nationwide Testing Availability
We have conveniently located testing centers across the United States, including major metropolitan areas such as New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our network of certified genetic counselors and neurological specialists ensures comprehensive care throughout your testing journey.
Pre-Test Requirements
Before scheduling your RUBCN gene test, please ensure:
- Complete clinical history documentation of the patient
- Genetic counseling session to create a detailed family pedigree chart
- Identification of affected family members for comprehensive analysis
Sample Collection and Processing
Our test accepts multiple sample types for your convenience:
- Blood samples collected by certified phlebotomists
- Extracted DNA from previous genetic testing
- Single drop of blood on FTA card for simplified collection
Turnaround Time: 3 to 4 weeks from sample receipt
Take Control of Your Neurological Health Today
Don’t let uncertainty about hereditary neurological conditions affect your quality of life. Our RUBCN Gene Salih Ataxia NGS Genetic DNA Test provides the clarity and confidence you need for informed healthcare decisions. With our discounted price of only $500 USD, advanced genetic testing is more accessible than ever.
Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic counseling session and book your test. Our dedicated team is ready to guide you through every step of the testing process and provide the answers you deserve.
