SEPT9 Gene Hereditary Neuralgic Amyotrophy NGS Genetic DNA Test
Comprehensive Genetic Testing for Hereditary Neuralgic Amyotrophy
The SEPT9 Gene Hereditary Neuralgic Amyotrophy NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics, offering precise detection of mutations associated with hereditary neuralgic amyotrophy (HNA). This advanced testing methodology provides crucial insights for individuals and families affected by this rare neurological condition, enabling early intervention and personalized management strategies.
What is Hereditary Neuralgic Amyotrophy?
Hereditary neuralgic amyotrophy is an inherited neurological disorder characterized by recurrent episodes of severe pain, muscle weakness, and sensory disturbances primarily affecting the shoulders, arms, and hands. These episodes can be triggered by various factors including infections, immunizations, stress, or physical exertion. The condition follows an autosomal dominant inheritance pattern, meaning a single copy of the mutated gene from either parent can cause the disorder.
What Does This Test Detect?
Our comprehensive NGS genetic test specifically targets mutations in the SEPT9 gene (septin 9), which has been identified as the primary genetic cause of hereditary neuralgic amyotrophy. The test analyzes:
- Point mutations and small insertions/deletions in the SEPT9 gene
- Copy number variations affecting gene function
- Specific pathogenic variants associated with HNA
- Genetic markers that influence disease severity and progression
Advanced NGS Technology
Utilizing state-of-the-art Next-Generation Sequencing technology, this test provides unparalleled accuracy in detecting genetic variations. NGS allows for comprehensive analysis of the entire SEPT9 gene with high sensitivity and specificity, ensuring reliable results for clinical decision-making.
Who Should Consider This Test?
Clinical Indications and Symptoms
This genetic test is recommended for individuals experiencing:
- Recurrent episodes of severe shoulder and arm pain
- Sudden onset muscle weakness in the upper extremities
- Sensory disturbances including numbness or tingling
- Muscle atrophy following painful episodes
- Family history of similar neurological symptoms
- Unexplained neurological symptoms with potential genetic basis
At-Risk Populations
- Individuals with confirmed family history of HNA
- Patients with atypical neurological presentations
- Couples planning pregnancy with family history of neurological disorders
- Individuals seeking definitive diagnosis for unexplained neurological symptoms
Benefits of SEPT9 Genetic Testing
Clinical Advantages
- Accurate Diagnosis: Provides definitive genetic confirmation of hereditary neuralgic amyotrophy
- Early Intervention: Enables proactive management before severe symptoms develop
- Personalized Treatment: Guides targeted therapeutic approaches based on genetic profile
- Family Planning: Informs reproductive decisions and genetic counseling
- Symptom Management: Helps anticipate and prepare for potential symptom flares
Long-Term Benefits
- Reduces diagnostic uncertainty and unnecessary testing
- Facilitates appropriate specialist referrals
- Supports comprehensive family risk assessment
- Enables participation in clinical trials and research studies
Understanding Your Test Results
Result Interpretation
Your genetic test results will fall into one of several categories:
- Positive Result: Indicates the presence of a known pathogenic mutation in the SEPT9 gene, confirming hereditary neuralgic amyotrophy diagnosis
- Negative Result: No pathogenic mutations detected, though clinical correlation remains important
- Variant of Uncertain Significance: Identifies genetic changes with unknown clinical impact requiring further evaluation
- Carrier Status: Important for family planning and genetic counseling purposes
Post-Test Guidance
All positive results include comprehensive genetic counseling to help you understand the implications for your health and family. Our genetic specialists provide:
- Detailed explanation of genetic findings
- Personalized management recommendations
- Family testing guidance
- Referrals to appropriate specialists
- Long-term monitoring strategies
Test Details and Pricing
| Test Information | Details |
|---|---|
| Test Name | SEPT9 Gene Hereditary Neuralgic Amyotrophy NGS Genetic DNA Test |
| Regular Price | $700 USD |
| Discount Price | $500 USD |
| Turnaround Time | 3 to 4 Weeks |
| Sample Type | Blood |
| Testing Method | Next-Generation Sequencing (NGS) |
Pre-Test Requirements
Before testing, we recommend:
- Comprehensive clinical history documentation
- Genetic counseling session to create detailed family pedigree
- Discussion of testing implications with healthcare provider
- Understanding of potential psychological impacts
Nationwide Testing Availability
We have diagnostic centers conveniently located across the United States, serving major metropolitan areas including:
- New York City and surrounding regions
- Los Angeles and Southern California
- Chicago and Midwest locations
- Houston and Texas facilities
- Miami and Florida centers
- Seattle and Pacific Northwest locations
- Boston and New England areas
- Atlanta and Southeastern regions
Take Control of Your Neurological Health
Don’t let uncertainty about hereditary neurological conditions affect your quality of life. Our SEPT9 Gene Hereditary Neuralgic Amyotrophy NGS Genetic DNA Test provides the clarity you need for informed healthcare decisions. With our discounted price of $500 USD (regularly $700 USD), advanced genetic testing is more accessible than ever.
Ready to take the next step in understanding your genetic health?
Call our genetic specialists today at +1(267) 388-9828 to schedule your test or discuss your testing options. Our team is available to answer your questions and guide you through the testing process.
Alternatively, you can WhatsApp us at the same number for convenient scheduling and information. Take advantage of our limited-time discount and gain valuable insights into your neurological health.
Early detection through genetic testing can make a significant difference in managing hereditary neuralgic amyotrophy and planning for your future health needs.
