Sale!

TCTN2 Gene Meckel Syndrome Type 8 NGS Genetic DNA Test

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

-29%

The TCTN2 Gene Meckel Syndrome Type 8 NGS Genetic DNA Test is a comprehensive genetic screening that identifies mutations in the TCTN2 gene associated with Meckel Syndrome Type 8. This advanced next-generation sequencing test provides crucial insights for individuals and families affected by this rare hereditary disorder that impacts multiple organ systems including liver, kidneys, and endocrine functions. The test helps in accurate diagnosis, family planning decisions, and personalized medical management strategies. With results available in 3-4 weeks from blood, extracted DNA, or FTA card samples, this test offers peace of mind and actionable genetic information. The discounted price is $500 USD, providing accessible genetic testing for those at risk of inheriting or carrying this condition.

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

TCTN2 Gene Meckel Syndrome Type 8 NGS Genetic DNA Test

Comprehensive Genetic Screening for Hereditary Disorders

The TCTN2 Gene Meckel Syndrome Type 8 NGS Genetic DNA Test represents a breakthrough in genetic diagnostics, offering precise detection of mutations in the TCTN2 gene responsible for Meckel Syndrome Type 8. This rare autosomal recessive disorder affects multiple organ systems and requires specialized genetic analysis for accurate diagnosis and management.

What Does This Test Measure?

This advanced genetic test utilizes Next-Generation Sequencing (NGS) technology to comprehensively analyze the TCTN2 gene for pathogenic variants associated with Meckel Syndrome Type 8. The test specifically identifies:

  • Point mutations and small insertions/deletions in the TCTN2 gene
  • Pathogenic variants affecting ciliary function and development
  • Genetic markers associated with multi-organ system involvement
  • Inheritance patterns for family planning decisions

Who Should Consider This Test?

Clinical Indications and Symptoms

This genetic test is recommended for individuals presenting with symptoms or family history suggestive of Meckel Syndrome Type 8, including:

  • Individuals with congenital anomalies affecting liver, kidneys, or endocrine systems
  • Patients with developmental delays and neurological abnormalities
  • Families with history of recurrent pregnancy loss or neonatal mortality
  • Couples planning pregnancy with family history of genetic disorders
  • Individuals with unexplained hepatic, renal, or endocrine dysfunction
  • Patients with characteristic facial features and skeletal abnormalities

Key Benefits of Genetic Testing

Undergoing the TCTN2 Gene Meckel Syndrome Type 8 NGS Genetic DNA Test provides numerous advantages:

  • Accurate Diagnosis: Provides definitive genetic confirmation for complex clinical presentations
  • Family Planning Guidance: Enables informed reproductive decisions and genetic counseling
  • Personalized Management: Facilitates targeted medical interventions and monitoring protocols
  • Early Intervention: Allows for proactive management of associated health complications
  • Peace of Mind: Reduces uncertainty and provides clarity for affected families

Understanding Your Test Results

Our comprehensive genetic counseling services help you interpret your results effectively:

  • Positive Result: Indicates presence of pathogenic TCTN2 gene mutations, confirming diagnosis and guiding management strategies
  • Negative Result: Suggests absence of detectable mutations, though clinical correlation remains essential
  • Variant of Uncertain Significance: Requires additional family studies and ongoing research correlation
  • Carrier Status: Identifies individuals who may pass the condition to offspring without showing symptoms

Test Details and Pricing

Test Component Details
Test Name TCTN2 Gene Meckel Syndrome Type 8 NGS Genetic DNA Test
Discount Price $500 USD
Regular Price $700 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, please ensure:

  • Complete clinical history documentation
  • Genetic counseling session to create detailed family pedigree
  • Understanding of test implications and potential outcomes
  • Informed consent for genetic testing procedures

Nationwide Accessibility

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 more cities. Our network of certified genetic counselors and healthcare professionals ensures comprehensive support throughout your testing journey.

Take the Next Step Toward Genetic Clarity

Don’t let uncertainty about genetic health conditions affect your family’s future. Our specialized genetic testing provides the answers you need for informed healthcare decisions and family planning. Contact our genetic counseling team today to schedule your TCTN2 Gene Meckel Syndrome Type 8 NGS Genetic DNA Test and take control of your genetic health.

Call or WhatsApp us today at +1(267) 388-9828 to book your appointment or discuss your genetic testing needs with our expert team.