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PDP1 Gene Pyruvate Dehydrogenase Phosphatase Deficiency Genetic Test

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

-29%

The PDP1 Gene Pyruvate Dehydrogenase Phosphatase Deficiency NGS Genetic DNA Test is a cutting-edge diagnostic tool that identifies mutations in the PDP1 gene responsible for pyruvate dehydrogenase phosphatase deficiency. This rare metabolic disorder affects the body’s ability to convert carbohydrates into energy, leading to severe neurological symptoms and developmental delays. Using Next-Generation Sequencing (NGS) technology, our test provides comprehensive analysis with 99% accuracy, enabling early diagnosis and personalized treatment strategies. The test is priced at $500 USD (discounted from $700) and is recommended for individuals with unexplained neurological symptoms, developmental delays, or family history of metabolic disorders. Results are typically available within 3-4 weeks, providing crucial information for managing this complex condition.

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PDP1 Gene Pyruvate Dehydrogenase Phosphatase Deficiency NGS Genetic DNA Test

Comprehensive Genetic Testing for Metabolic Disorders

The PDP1 Gene Pyruvate Dehydrogenase Phosphatase Deficiency NGS Genetic DNA Test represents a breakthrough in genetic diagnostics for rare metabolic disorders. This advanced test specifically targets mutations in the PDP1 gene, which plays a critical role in regulating the pyruvate dehydrogenase complex – a fundamental enzyme system responsible for converting carbohydrates into usable cellular energy. When this regulatory mechanism fails, it leads to severe metabolic disturbances that can significantly impact neurological development and overall health.

What This Test Measures and Detects

Our comprehensive NGS-based test analyzes the entire coding region of the PDP1 gene to identify:

  • Point mutations and single nucleotide variants
  • Small insertions and deletions
  • Copy number variations
  • Regulatory region abnormalities
  • Pathogenic variants affecting enzyme function

The test utilizes Next-Generation Sequencing technology, providing unparalleled accuracy and comprehensive coverage of the PDP1 gene with 99% analytical sensitivity. This ensures reliable detection of even rare genetic variants that might be missed by conventional testing methods.

Who Should Consider This Test

This genetic test is particularly recommended for individuals presenting with:

  • Unexplained neurological symptoms in infancy or childhood
  • Developmental delays and cognitive impairment
  • Epileptic seizures unresponsive to standard treatments
  • Hypotonia (reduced muscle tone) and muscle weakness
  • Lactic acidosis episodes
  • Abnormal brain imaging findings
  • Family history of metabolic disorders
  • Siblings of affected individuals for carrier screening

Clinical Benefits of Early Detection

Early diagnosis through genetic testing provides numerous advantages:

  • Personalized Treatment Planning: Enables targeted therapeutic interventions
  • Family Planning Guidance: Provides crucial information for genetic counseling
  • Proactive Management: Allows for early intervention to minimize complications
  • Accurate Prognosis: Helps predict disease progression and outcomes
  • Reduced Diagnostic Odyssey: Eliminates unnecessary testing and medical procedures

Understanding Your Test Results

Our comprehensive genetic counseling support helps you interpret your results:

  • Positive Result: Indicates the presence of pathogenic mutations in the PDP1 gene, confirming the diagnosis of pyruvate dehydrogenase phosphatase deficiency
  • Negative Result: Suggests that no disease-causing mutations were detected in the PDP1 gene
  • Variant of Uncertain Significance: Identifies genetic changes whose clinical significance is currently unknown, requiring further evaluation

All results are accompanied by detailed explanations and recommendations from our certified genetic counselors to ensure complete understanding and appropriate next steps.

Test Pricing and Details

Test Component Details
Test Name PDP1 Gene Pyruvate Dehydrogenase Phosphatase Deficiency NGS Genetic DNA Test
Regular Price $700 USD
Discount Price $500 USD
Turnaround Time 3 to 4 Weeks
Sample Type Blood, Extracted DNA, or One Drop Blood on FTA Card
Testing Method Next-Generation Sequencing (NGS) Technology

Pre-Test Requirements

Before scheduling your test, we recommend:

  • Complete clinical history documentation
  • Genetic counseling session to create a detailed family pedigree
  • Discussion of testing implications with healthcare provider
  • Understanding of potential outcomes and their significance

Nationwide Accessibility

We have diagnostic centers conveniently located across the United States, including major metropolitan areas such as New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many more. Our network ensures that quality genetic testing is accessible to patients nationwide.

Take the Next Step Toward Diagnosis

Don’t let uncertainty about metabolic symptoms delay proper diagnosis and treatment. Our PDP1 Gene Pyruvate Dehydrogenase Phosphatase Deficiency NGS Genetic DNA Test provides the clarity needed for effective management of this complex condition. With our discounted price of $500 USD and comprehensive genetic counseling support, you can make informed decisions about your health or your child’s health.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic test consultation and take the first step toward accurate diagnosis and personalized care.