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RAD51 Gene Mirror Movements Type 2 Genetic Test

Original price was: $700.Current price is: $500.

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The RAD51 Gene Mirror Movements Type 2 NGS Genetic DNA Test is a specialized genetic analysis that identifies mutations in the RAD51 gene associated with mirror movements type 2, a rare neurological condition characterized by involuntary movements that mirror voluntary actions on the opposite side of the body. This comprehensive test utilizes next-generation sequencing (NGS) technology to provide precise genetic information crucial for diagnosis and family planning. Individuals experiencing involuntary mirroring movements, those with family history of neurological disorders, or patients with unexplained movement abnormalities should consider this test. The test offers definitive diagnosis, enables personalized treatment planning, provides valuable information for family members, and helps guide reproductive decisions. Results are typically available within 3-4 weeks and require a simple blood sample or extracted DNA. The test is priced at $500 USD with a regular price of $700 USD, making advanced genetic testing accessible for comprehensive neurological evaluation.

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RAD51 Gene Mirror Movements Type 2 NGS Genetic DNA Test

Comprehensive Genetic Analysis for Neurological Movement Disorders

The RAD51 Gene Mirror Movements Type 2 NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics, specifically designed to identify mutations in the RAD51 gene that cause mirror movements type 2. This rare neurological condition manifests as involuntary movements that mirror voluntary actions performed on the opposite side of the body, creating significant challenges in daily functioning and quality of life.

What This Advanced Genetic Test Detects

Our cutting-edge NGS (Next-Generation Sequencing) technology precisely analyzes the RAD51 gene to identify pathogenic variants responsible for mirror movements type 2. The test examines:

  • Complete RAD51 gene sequencing for comprehensive mutation detection
  • Specific genetic markers associated with neurological movement disorders
  • Inheritance patterns and familial risk assessment
  • Variant classification according to international genetic standards

Who Should Consider This Genetic Test?

This specialized genetic analysis is recommended for individuals experiencing:

  • Involuntary mirroring movements during voluntary actions
  • Family history of neurological movement disorders
  • Unexplained coordination difficulties or abnormal movements
  • Children showing developmental movement abnormalities
  • Individuals with suspected inherited neurological conditions
  • Patients undergoing neurological evaluation for movement disorders

Clinical Symptoms and Indications

Mirror movements type 2 typically presents with specific clinical features including involuntary movements that precisely mirror voluntary actions on the contralateral side. These movements often affect hand coordination, fine motor skills, and can significantly impact daily activities such as writing, eating, and self-care tasks.

Significant Benefits of RAD51 Genetic Testing

  • Definitive Diagnosis: Provides conclusive genetic confirmation of mirror movements type 2
  • Personalized Treatment Planning: Enables targeted therapeutic interventions based on genetic findings
  • Family Risk Assessment: Identifies inheritance patterns and risk for family members
  • Reproductive Guidance: Supports informed family planning decisions
  • Early Intervention: Facilitates timely management strategies for better outcomes
  • Research Contribution: Advances understanding of rare neurological conditions

Understanding Your Test Results

Our comprehensive genetic counseling services help you interpret your RAD51 gene test results with clarity and confidence:

  • Positive Result: Indicates the presence of a pathogenic RAD51 gene mutation associated with mirror movements type 2
  • Negative Result: Suggests no detectable mutation in the RAD51 gene, though clinical evaluation remains important
  • Variant of Uncertain Significance: Identifies genetic changes requiring further clinical correlation
  • Carrier Status: Determines if you carry the genetic mutation without showing symptoms

All results include detailed interpretation by our board-certified genetic specialists and neurologists, ensuring you receive comprehensive guidance for next steps in management and care.

Test Pricing and Availability

Test Component Price (USD)
Discount Price $500
Regular Price $700

Nationwide Accessibility

We proudly serve patients across the United States with convenient testing locations in major cities including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our network of certified collection centers ensures accessible genetic testing services nationwide.

Pre-Test Requirements and Sample Collection

To ensure accurate results, please prepare:

  • Complete clinical history documentation
  • Genetic counseling session for family pedigree analysis
  • Blood sample, extracted DNA, or one drop of blood on FTA card
  • 3-4 week turnaround time for comprehensive analysis

Take Control of Your Neurological Health Today

Don’t let uncertainty about movement disorders affect your quality of life. Our RAD51 Gene Mirror Movements Type 2 NGS Genetic DNA Test provides the clarity and answers you need for proper diagnosis and management. With advanced NGS technology and expert genetic analysis, you can make informed decisions about your neurological health.

Call or WhatsApp us now at +1(267) 388-9828 to schedule your genetic testing appointment. Our dedicated genetic counselors are available to answer your questions and guide you through the testing process with compassion and expertise.

Book your RAD51 genetic test today and take the first step toward understanding your neurological health with precision and confidence.