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FOXH1 Gene Congenital Heart Disease and Transposition of the Great Arteries NGS Genetic DNA Test

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

-29%

The FOXH1 Gene Congenital Heart Disease and Transposition of the Great Arteries NGS Genetic DNA Test is a cutting-edge diagnostic tool that identifies mutations in the FOXH1 gene associated with serious congenital heart conditions. This comprehensive test utilizes Next-Generation Sequencing (NGS) technology to provide detailed genetic analysis for individuals and families with histories of congenital heart defects. The test is particularly valuable for pediatric patients showing symptoms of cardiac abnormalities or those with family histories of transposition of the great arteries. Results provide crucial information for medical management, surgical planning, and family genetic counseling. The test costs $500 USD and offers significant benefits including early intervention opportunities, personalized treatment strategies, and informed family planning decisions.

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FOXH1 Gene Congenital Heart Disease and Transposition of the Great Arteries NGS Genetic DNA Test

Comprehensive Genetic Testing for Congenital Heart Conditions

The FOXH1 Gene Congenital Heart Disease and Transposition of the Great Arteries NGS Genetic DNA Test represents a significant advancement in pediatric cardiology and genetic diagnostics. This specialized test focuses on identifying mutations in the FOXH1 gene, which plays a crucial role in embryonic heart development and has been linked to serious congenital heart defects, particularly transposition of the great arteries (TGA).

What Does This Test Measure?

This advanced genetic screening utilizes Next-Generation Sequencing (NGS) technology to comprehensively analyze the FOXH1 gene for:

  • Point mutations and single nucleotide variants
  • Insertions and deletions within the gene sequence
  • Regulatory region abnormalities affecting gene expression
  • Pathogenic variants associated with congenital heart disease
  • Specific mutations linked to transposition of the great arteries

Who Should Consider This Test?

This genetic test is recommended for individuals displaying the following indications:

  • Newborns or infants with suspected congenital heart defects
  • Children diagnosed with transposition of the great arteries
  • Patients with family histories of congenital heart disease
  • Individuals with multiple congenital anomalies involving cardiac structures
  • Parents planning pregnancy with previous children affected by heart defects
  • Patients undergoing evaluation for dysmorphology syndromes

Key Benefits of FOXH1 Genetic Testing

  • Early Diagnosis: Enables prompt identification of genetic predispositions to congenital heart conditions
  • Personalized Treatment: Guides surgical planning and medical management strategies
  • Family Planning: Provides valuable information for genetic counseling and reproductive decisions
  • Proactive Monitoring: Allows for early intervention and specialized cardiac care
  • Comprehensive Analysis: Utilizes state-of-the-art NGS technology for accurate results

Understanding Your Test Results

Your genetic test results will be carefully interpreted by our team of certified genetic counselors and pediatric cardiologists:

  • Positive Result: Indicates the presence of a FOXH1 gene mutation associated with congenital heart disease risk
  • Negative Result: Suggests no detectable mutations in the FOXH1 gene, though other genetic factors may still be present
  • Variant of Uncertain Significance: Some genetic changes may require additional family studies for proper interpretation
  • Clinical Correlation: Results should always be interpreted in the context of clinical symptoms and family history

Test Pricing Information

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

Test Specifications

  • Turnaround Time: 3 to 4 Weeks
  • Sample Type: Blood, Extracted DNA, or One Drop Blood on FTA Card
  • Methodology: Next-Generation Sequencing (NGS) Technology
  • Specialty: Pediatrics
  • Department: Genetics
  • Disease Focus: Dysmorphology and Congenital Heart Defects

Pre-Test Requirements

Before scheduling your test, please ensure:

  • Complete clinical history documentation of the patient
  • Genetic counseling session to create a detailed family pedigree chart
  • Documentation of family members affected by congenital heart conditions
  • Review of previous cardiac evaluations and imaging studies

Nationwide Accessibility

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 comprehensive network ensures accessible genetic testing services for families nationwide.

Take Action for Your Family’s Heart Health

Don’t wait to get the answers you need about congenital heart disease risks. Our specialized genetic testing provides crucial information for managing cardiac health and making informed medical decisions. Contact our genetic counseling team today to schedule your FOXH1 gene test and take the first step toward comprehensive cardiac care.

Book Your Test Today: Call or WhatsApp our genetic specialists at +1(267) 388-9828 to schedule your appointment and receive personalized guidance throughout the testing process.