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Nx Gen Sequencing Episodic Ataxia Test

Original price was: $650.Current price is: $586.

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The Nx Gen Sequencing Episodic Ataxia Test is a comprehensive genetic analysis that identifies mutations in key genes associated with episodic ataxia disorders. This advanced diagnostic tool utilizes next-generation sequencing technology to detect variations in CACNA1A, CACNB4, GABRD, GABRG2, KCNA1, SCN1A, SCN1B, SCN2A, SCN9A, and SLC1A3 genes. The test is essential for individuals experiencing recurrent episodes of poor coordination, balance problems, dizziness, or vertigo. Benefits include accurate diagnosis, personalized treatment planning, and genetic counseling insights. The test costs $586 USD with a regular price of $650 USD, providing significant savings for comprehensive neurological genetic testing.

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Nx Gen Sequencing Episodic Ataxia Test

Comprehensive Genetic Testing for Episodic Ataxia Disorders

The Nx Gen Sequencing Episodic Ataxia Test represents a breakthrough in neurological genetic diagnostics, offering unparalleled accuracy in identifying the genetic underpinnings of episodic ataxia disorders. Episodic ataxia comprises a group of rare neurological conditions characterized by recurrent episodes of poor coordination, balance disturbances, and movement difficulties. These episodes can significantly impact daily life and often require precise diagnosis for effective management.

What This Advanced Test Measures

Our state-of-the-art Nx Gen Sequencing technology comprehensively analyzes ten critical genes associated with episodic ataxia:

  • CACNA1A – Calcium voltage-gated channel subunit alpha1 A
  • CACNB4 – Calcium voltage-gated channel auxiliary subunit beta 4
  • GABRD – Gamma-aminobutyric acid type A receptor delta subunit
  • GABRG2 – Gamma-aminobutyric acid type A receptor gamma2 subunit
  • KCNA1 – Potassium voltage-gated channel subfamily A member 1
  • SCN1A – Sodium voltage-gated channel alpha subunit 1
  • SCN1B – Sodium voltage-gated channel beta subunit 1
  • SCN2A – Sodium voltage-gated channel alpha subunit 2
  • SCN9A – Sodium voltage-gated channel alpha subunit 9
  • SLC1A3 – Solute carrier family 1 member 3

Who Should Consider This Genetic Test

This comprehensive genetic analysis is recommended for individuals experiencing:

  • Recurrent episodes of unsteady gait and poor coordination
  • Periodic dizziness or vertigo without apparent cause
  • Family history of episodic movement disorders
  • Intermittent balance problems affecting daily activities
  • Unexplained neurological symptoms that come and go
  • Previous inconclusive neurological evaluations

Significant Benefits of Genetic Testing

Undergoing the Nx Gen Sequencing Episodic Ataxia Test provides numerous advantages:

  • Accurate Diagnosis: Precise identification of specific genetic mutations
  • Personalized Treatment: Targeted therapeutic approaches based on genetic findings
  • Family Planning: Genetic counseling for inheritance patterns and risk assessment
  • Symptom Management: Better understanding of triggers and preventive strategies
  • Prognostic Information: Insights into disease progression and potential complications
  • Research Contribution: Participation in advancing neurological genetic knowledge

Understanding Your Test Results

Our comprehensive report provides detailed analysis of your genetic profile:

  • Positive Result: Identifies specific genetic mutations associated with episodic ataxia, enabling targeted treatment and management strategies
  • Negative Result: Rules out common genetic causes, helping narrow diagnostic possibilities
  • Variant of Uncertain Significance: Identifies genetic changes requiring further clinical correlation
  • Carrier Status: Information about recessive inheritance patterns when relevant

All results are accompanied by detailed interpretation from our expert genetic counselors and neurologists, ensuring you receive comprehensive guidance for next steps.

Test Pricing and Details

Test Component Price (USD)
Nx Gen Sequencing Episodic Ataxia Test $586 (Discounted from $650)
Turnaround Time 40 Working Days (Samples processed daily by 9 AM)
Sample Requirements 10 mL (5 mL minimum) whole blood from 2 Lavender Top (EDTA) tubes
Shipping Instructions Ship refrigerated. DO NOT FREEZE
Required Documentation Duly filled Whole Exome Sequencing Consent Form (Form 37)

Nationwide Testing Availability

We proudly serve patients across the United States with convenient testing locations in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, Austin, Jacksonville, Fort Worth, Columbus, San Francisco, and many more. Our network ensures accessible genetic testing services regardless of your location.

Take Control of Your Neurological Health

Don’t let unexplained neurological symptoms control your life. The Nx Gen Sequencing Episodic Ataxia Test provides the clarity needed for proper diagnosis and effective management. Our advanced genetic testing technology, combined with expert interpretation, offers the comprehensive insights necessary for informed healthcare decisions.

Ready to begin your diagnostic journey? Book your Nx Gen Sequencing Episodic Ataxia Test today by calling our dedicated genetics specialists at +1(267) 388-9828 or schedule your appointment online. Take the first step toward understanding your neurological health with confidence and precision.