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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 comprehensive diagnostic tool that identifies mutations in the PRKD1 gene associated with complex developmental disorders. This advanced next-generation sequencing test provides precise detection of genetic variants responsible for congenital heart abnormalities and ectodermal dysplasia manifestations. The test is crucial for individuals presenting with cardiac malformations, distinctive facial features, and skin/hair abnormalities. Results offer valuable insights for personalized medical management, family planning decisions, and targeted therapeutic interventions. With a turnaround time of 3-4 weeks and requiring only blood or extracted DNA samples, this $500 USD test represents a significant advancement in genetic diagnostics for rare congenital conditions.

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  • Trusted by Hospitals & Patients —Accredited Testing with Results
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PRKD1 Gene Congenital Heart Defects and Ectodermal Dysplasia NGS Genetic DNA Test

Comprehensive Genetic Analysis for Complex Developmental 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 rare congenital conditions. This sophisticated test utilizes next-generation sequencing technology to provide comprehensive analysis of the PRKD1 gene, which plays a critical role in embryonic development and tissue formation.

What This Advanced Genetic Test Detects

Our NGS-based PRKD1 gene test specifically identifies pathogenic variants and mutations within the PRKD1 gene that are responsible for:

  • Congenital heart defects including septal abnormalities and structural malformations
  • Ectodermal dysplasia manifestations affecting skin, hair, and nails
  • Distinctive facial dysmorphic features
  • Developmental delays and growth abnormalities
  • Inherited genetic patterns affecting multiple organ systems

Who Should Consider PRKD1 Genetic Testing?

This comprehensive genetic evaluation is recommended for individuals presenting with:

Clinical Indications and Symptoms

  • Newborns or children with congenital heart abnormalities detected at birth
  • Individuals with characteristic ectodermal dysplasia features including sparse hair, abnormal tooth development, and skin abnormalities
  • Patients with distinctive facial features suggestive of genetic syndromes
  • Family history of PRKD1-related disorders or similar congenital conditions
  • Unexplained developmental delays with cardiac and ectodermal involvement
  • Individuals planning pregnancy with family history of congenital heart defects

Significant Benefits of PRKD1 Genetic Testing

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

Medical Management Advantages

  • Accurate Diagnosis: Provides definitive genetic confirmation for complex clinical presentations
  • Personalized Treatment: Enables targeted medical interventions and specialized care planning
  • Family Planning Guidance: Offers valuable information for reproductive decision-making
  • Early Intervention: Facilitates proactive management of associated health complications
  • Genetic Counseling: Supports informed family discussions about inheritance patterns
  • Research Contribution: Advances understanding of rare genetic disorders

Understanding Your Test Results

Our comprehensive genetic counseling support helps you interpret your PRKD1 test findings:

Result Interpretation Guidance

  • Positive Result: Indicates presence of pathogenic PRKD1 mutation, confirming genetic diagnosis and enabling targeted management
  • Negative Result: Suggests absence of detectable PRKD1 mutations, though clinical evaluation remains important
  • Variant of Uncertain Significance: Identifies genetic changes requiring further clinical correlation and monitoring
  • Carrier Status: Determines inheritance patterns and reproductive risks for family members

Test Details and Pricing

Test Component Details
Test Name PRKD1 Gene Congenital Heart Defects and Ectodermal Dysplasia NGS Genetic DNA Test
Discount Price $500 USD
Regular Price $700 USD
Turnaround Time 3 to 4 Weeks
Sample Type Blood or Extracted DNA or One drop Blood on FTA Card
Specialty Pediatrics
Department Genetics
Method NGS Technology
Disease Type Dysmorphology

Pre-Test Preparation Requirements

To ensure optimal testing outcomes, please prepare the following:

  • Complete clinical history documentation of the patient
  • Genetic counseling session to establish family pedigree chart
  • Documentation of affected family members with similar conditions
  • Recent medical evaluations and diagnostic imaging reports

Nationwide Testing Availability

We provide comprehensive genetic testing services across the United States with convenient 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 accessible, high-quality care regardless of your location.

Schedule Your Genetic Evaluation Today

Take the first step toward comprehensive genetic understanding and personalized medical management. Our team of genetic specialists is ready to guide you through the testing process and provide expert interpretation of your results.

Call or WhatsApp us now at +1(267) 388-9828 to schedule your PRKD1 genetic test consultation and begin your journey toward accurate diagnosis and targeted treatment planning.