Sale!

PRKD1 Gene Congenital Heart Defects and Ectodermal Dysplasia NGS Genetic DNA Test

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

-29%

The PRKD1 Gene Congenital Heart Defects and Ectodermal Dysplasia NGS Genetic DNA Test is a specialized diagnostic tool that identifies mutations in the PRKD1 gene associated with rare genetic disorders. This comprehensive test utilizes Next-Generation Sequencing (NGS) technology to detect genetic variations that cause congenital heart abnormalities and ectodermal dysplasia symptoms. The test is crucial for individuals with family history of these conditions, unexplained cardiac defects, or developmental abnormalities affecting skin, hair, and teeth. Results provide valuable information for medical management, family planning, and personalized treatment approaches. The test costs $500 USD and includes professional genetic counseling to help interpret findings and understand inheritance patterns.

Clinically Validated & Lab Certified

  • ISO-Accredited Laboratory, Ensuring Highest Standards
  • Trusted by Hospitals & Patients —Accredited Testing with Results
  • Direct Healthcare Provider Support + Comprehensive Reporting
Guaranteed Safe Checkout

PRKD1 Gene Congenital Heart Defects and Ectodermal Dysplasia NGS Genetic DNA Test

Comprehensive Genetic Testing for Rare Disorders

The PRKD1 Gene Congenital Heart Defects and Ectodermal Dysplasia NGS Genetic DNA Test represents a cutting-edge diagnostic approach for identifying genetic mutations associated with complex developmental disorders. This specialized test focuses on the PRKD1 gene, which plays a critical role in embryonic development and cellular signaling pathways. Mutations in this gene have been linked to a spectrum of congenital abnormalities affecting both cardiovascular and ectodermal systems.

What Does This Test Measure?

Our advanced NGS technology provides comprehensive analysis of the PRKD1 gene to detect:

  • Point mutations and single nucleotide variants
  • Small insertions and deletions (indels)
  • Copy number variations affecting the PRKD1 locus
  • Structural rearrangements within the gene region
  • Pathogenic variants associated with congenital heart disease
  • Mutations linked to ectodermal dysplasia manifestations

Who Should Consider This Test?

This genetic test is recommended for individuals presenting with:

  • Unexplained congenital heart defects including septal defects, valve abnormalities, or complex cardiac malformations
  • Developmental abnormalities affecting skin, hair, nails, or teeth
  • Family history of PRKD1-related disorders or similar genetic conditions
  • Multiple congenital anomalies involving both cardiac and ectodermal systems
  • Unexplained developmental delays with cardiac involvement
  • Previous inconclusive genetic testing for congenital disorders

Clinical Benefits of PRKD1 Genetic Testing

Undergoing PRKD1 genetic testing provides numerous advantages for patients and families:

  • Accurate Diagnosis: Provides definitive genetic confirmation for complex clinical presentations
  • Family Planning Guidance: Enables informed reproductive decisions through understanding inheritance patterns
  • Personalized Medical Management: Guides specialized cardiac and dermatological care based on genetic findings
  • Prognostic Information: Helps predict disease progression and potential complications
  • Early Intervention Opportunities: Facilitates timely medical and surgical interventions when indicated
  • Psychological Relief: Reduces diagnostic uncertainty and provides closure for families

Understanding Your Test Results

Our comprehensive genetic counseling services help you interpret your PRKD1 test results:

  • Positive Result: Indicates the presence of a pathogenic PRKD1 mutation. Our genetic counselors will explain the specific variant, inheritance pattern, and implications for medical management.
  • Negative Result: Suggests no disease-causing PRKD1 mutations were detected. However, other genetic or environmental factors may still contribute to symptoms.
  • Variant of Uncertain Significance (VUS): Identifies genetic changes with unclear clinical impact. Ongoing research may provide additional insights over time.
  • Carrier Status: Determines if you carry a single copy of a PRKD1 mutation, which may have implications for family planning.

Test Pricing and Details

Test Feature Details
Test Name PRKD1 Gene Congenital Heart Defects and Ectodermal Dysplasia 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

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, and many other cities. Our network of certified genetic counselors and medical professionals ensures consistent, high-quality care regardless of your location.

Take the Next Step Toward Genetic Clarity

Don’t let uncertainty about genetic conditions affect your health decisions. Our PRKD1 genetic testing provides the answers you need for informed medical care and family planning. With our discounted price of $500 USD and comprehensive genetic counseling services, you’ll receive expert guidance every step of the way.

Ready to schedule your test? Contact our genetic specialists today at +1(267) 388-9828 or book your appointment online. Our team is available to answer your questions and help you understand the testing process.