Sale!

PC Gene Pyruvate Carboxylase Deficiency Genetic Test

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

-29%

The PC Gene Pyruvate Carboxylase Deficiency NGS Genetic DNA Test is a cutting-edge diagnostic tool that identifies mutations in the PC gene responsible for pyruvate carboxylase deficiency, a rare metabolic disorder affecting the nervous system. This comprehensive test utilizes Next-Generation Sequencing (NGS) technology to provide accurate detection of genetic variants that disrupt normal energy metabolism in the brain and other tissues. Patients experiencing unexplained neurological symptoms, developmental delays, or metabolic crises can benefit from this precise genetic analysis. The test costs $500 USD and provides results within 3-4 weeks, offering crucial information for treatment planning and genetic counseling. Early detection through this advanced genetic testing can significantly improve patient outcomes and guide appropriate therapeutic interventions for this complex neurological condition.

Trusted Testing. Expert Care. Guaranteed Privacy.

  • Accredited and Trusted
  • Expert Scientists, Advanced Technology
  • Data Privacy Guaranteed
Guaranteed Safe Checkout

PC Gene Pyruvate Carboxylase Deficiency NGS Genetic DNA Test

Comprehensive Genetic Testing for Neurological Metabolic Disorders

The PC Gene Pyruvate Carboxylase Deficiency NGS Genetic DNA Test represents a breakthrough in diagnostic precision for rare metabolic neurological conditions. This advanced genetic analysis specifically targets mutations in the PC gene, which encodes the pyruvate carboxylase enzyme essential for proper energy metabolism in the central nervous system. By utilizing cutting-edge Next-Generation Sequencing technology, our test provides unparalleled accuracy in detecting genetic variants that could lead to serious neurological complications if left undiagnosed.

What This Test Measures and Detects

Our comprehensive NGS genetic test specifically analyzes:

  • Complete sequencing of the PC gene for pathogenic variants
  • Detection of missense, nonsense, frameshift, and splice-site mutations
  • Identification of both inherited and de novo genetic alterations
  • Assessment of variant pathogenicity and clinical significance
  • Evaluation of genotype-phenotype correlations for personalized insights

Who Should Consider This Genetic Test

This specialized genetic testing is recommended for individuals presenting with:

  • Unexplained neurological symptoms in infancy or early childhood
  • Developmental delays and regression of motor skills
  • Metabolic acidosis episodes without clear cause
  • Family history of pyruvate carboxylase deficiency or related disorders
  • Abnormal neurological findings with suspected metabolic etiology
  • Unexplained seizures or encephalopathy episodes
  • Failure to thrive with neurological manifestations

Key Benefits of PC Gene Testing

Choosing our comprehensive genetic analysis provides numerous advantages:

  • Early and Accurate Diagnosis: Precise identification of PC gene mutations enables timely intervention
  • Personalized Treatment Planning: Results guide targeted therapeutic approaches and management strategies
  • Family Planning Guidance: Essential information for genetic counseling and reproductive decisions
  • Prognostic Insights: Understanding disease severity and potential progression patterns
  • Comprehensive Genetic Profile: Detailed analysis using state-of-the-art NGS technology

Understanding Your Test Results

Our genetic specialists provide comprehensive interpretation of your results:

  • Positive Result: Indicates presence of pathogenic PC gene mutations, confirming diagnosis and guiding specific treatment protocols
  • Negative Result: Suggests absence of known pathogenic variants, though clinical correlation remains essential
  • Variant of Uncertain Significance: Requires additional family studies and ongoing research correlation
  • Carrier Status: Identifies individuals with single mutation copies who may pass the condition to offspring

Test Pricing and Details

Test Component Price (USD)
Discount Price $500
Regular Price $700
Turnaround Time 3 to 4 Weeks
Sample Type Blood, Extracted DNA, or One Drop Blood on FTA Card

Pre-Test Requirements

Before scheduling your test, please ensure:

  • Complete clinical history documentation of the patient
  • Genetic counseling session to create detailed family pedigree chart
  • Identification of affected family members for comprehensive analysis
  • Understanding of test implications and potential outcomes

Nationwide Testing Availability

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

Take Control of Your Neurological Health

Don’t let unexplained neurological symptoms remain a mystery. Our PC Gene Pyruvate Carboxylase Deficiency NGS Genetic DNA Test provides the clarity needed for proper diagnosis and management. With our discounted price of $500 and comprehensive analysis, you can make informed decisions about your neurological health.

Ready to schedule your genetic test? Call our genetic specialists today at +1(267) 388-9828 or book your appointment online. Take the first step toward understanding your genetic profile and optimizing your neurological care.