Understand Neurological Risk
Before Symptoms Shape the Future
Gene Panel
164 Neurological Genes
Sample Type
Buccal Swab / Saliva
Identify clinically relevant genetic variants associated with hereditary neurological disorders to support earlier diagnosis, personalized treatment, and informed family planning.
Why Neurological Genetic
Testing Matters
Genetic testing helps identify hereditary neurological risks before symptoms appear, helping providers:
- diagnose earlier
- personalize treatments
- assess future risk
- support family planning
- evaluate clinical trial eligibility
Synaptic Transmission
Neurotransmitter release, transport, and synaptic cleft signaling pathways.
Myelin Sheath Integrity
Axonal insulation, conduction speeds, and peripheral myelin integrity.
Ion Channel Conduction
Action potentials, voltage-gated sodium, potassium, and calcium pathways.
Protein Folding & Clearing
Amyloid processing, synuclein clearing, and cellular toxic aggregations.
Early Diagnosis
Identify neurological risks before symptom progression.
Accurate Diagnosis
Clarify complex neurological conditions.
Personalized Treatment
Target therapies based on genetics.
Family Planning
Understand inherited neurological risk.
Prognostic Insights
Prepare for future disease progression.
Clinical Trial Access
Identify eligibility for emerging therapies.
Neurological Conditions We Assess
Precision screening and diagnostic clarity across complex inherited neurological pathologies.
Alzheimer's Disease
Huntington's Disease
Parkinson's Disease
ALS
Epilepsy
Charcot-Marie-Tooth Disease
Rett Syndrome
Ataxia
Comprehensive 164-Gene Neurological Panel
Broad genomic analysis across clinically relevant neurological genes to support precision diagnosis and proactive neurological care.
How Neurological Genetic Testing Works
Clinical Evaluation
Discuss symptoms, history, and testing suitability.
Sample Collection
Simple saliva or buccal swab collection.
Genomic Sequencing
Advanced neurological gene analysis.
Variant Interpretation
Likely pathogenic and pathogenic variants identified.
Personalized Clinical Guidance
Actionable recommendations for care planning.
What Happens After a Positive Result?
Confirm Diagnosis
Additional clinical evaluations.
Inform Family
Understand hereditary implications.
Personalized Care Plan
Medication, therapy, lifestyle.
Ongoing Monitoring
Long-term neurological tracking.
Genetic Counseling
Family planning support.
The Power of Neurological Genetic Testing
Diagnose Earlier
Earlier detection improves outcomes.
Family Planning
Understand hereditary transmission.
Risk Reduction
Take proactive action sooner.
Personalized Treatment
Tailored neurological care.
Assay Specifications
& Performance Metrics
Sample Type
Buccal Swab / Saliva
Turnaround Time
7–10 Business Days
Coverage
>96% at 20x
Reporting
Pathogenic Variants
Customization
Custom Gene List
Panel Size
164 Genes
Why Choose Vediagnostics
for Neurogenomic Testing?
High-Quality Testing
Advanced neurological genomics.
Fast Turnaround
Rapid clinical reporting.
Comprehensive Panels
Wide neurological disorder coverage.
Provider Collaboration
Precision physician support.
Understanding Neurological
Genetic Testing
Built for Neurology &
Precision Clinical Care
Vediagnostics simplifies clinical laboratory management with provider access portal requisitions, rapid diagnostics turnaround, and comprehensive genetic mapping.
Transform Neurological Care
Through Genetic Understanding
Enable earlier intervention, informed decisions, and personalized neurological care through advanced hereditary risk testing.