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TSPYL1 Gene Sudden Infant Death with Dysgenesis of the Testes Syndrome NGS Genetic DNA Test

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

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The TSPYL1 Gene Sudden Infant Death with Dysgenesis of the Testes Syndrome NGS Genetic DNA Test is a comprehensive diagnostic tool that identifies mutations in the TSPYL1 gene associated with this rare genetic disorder. This test utilizes Next-Generation Sequencing (NGS) technology to provide accurate detection of genetic variants that can cause sudden infant death syndrome combined with testicular developmental abnormalities. The test is crucial for families with a history of unexplained infant deaths or reproductive system disorders. Results are typically available within 3-4 weeks from sample collection. The test costs $500 USD and requires either blood, extracted DNA, or one drop of blood on an FTA card. Genetic counseling is recommended before testing to understand family history and potential implications.

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TSPYL1 Gene Sudden Infant Death with Dysgenesis of the Testes Syndrome NGS Genetic DNA Test

Understanding TSPYL1 Gene Testing

The TSPYL1 Gene Sudden Infant Death with Dysgenesis of the Testes Syndrome NGS Genetic DNA Test represents a breakthrough in genetic diagnostics for rare inherited disorders affecting both cardiovascular and reproductive systems. This comprehensive genetic analysis targets the TSPYL1 gene, which plays a critical role in cellular regulation and development. When mutations occur in this gene, they can lead to severe medical conditions characterized by sudden unexpected infant death combined with abnormal testicular development.

What Does This Test Measure?

This advanced genetic test specifically detects:

  • Pathogenic variants in the TSPYL1 gene sequence
  • Single nucleotide polymorphisms (SNPs) associated with disease risk
  • Insertions, deletions, and other structural variations
  • Copy number variations affecting gene function
  • Regulatory region mutations impacting gene expression

Who Should Consider This Test?

This genetic test is particularly important for individuals and families experiencing:

  • Unexplained sudden infant death in family history
  • Male infants with abnormal testicular development
  • Families with multiple cases of infant mortality
  • Couples planning pregnancy with family history of genetic disorders
  • Individuals with suspected inherited cardiovascular conditions
  • Patients with reproductive system abnormalities of unknown origin

Clinical Symptoms and Indications

Healthcare providers may recommend this test when patients present with:

  • History of sudden unexpected infant death syndrome
  • Cryptorchidism (undescended testes) in male infants
  • Abnormal genital development
  • Family patterns suggesting inherited disorders
  • Unexplained cardiac events in infancy
  • Developmental delays with reproductive system concerns

Benefits of TSPYL1 Genetic Testing

Undergoing this comprehensive genetic analysis provides numerous advantages:

  • Accurate Diagnosis: Provides definitive identification of TSPYL1 gene mutations
  • Family Planning Guidance: Enables informed reproductive decisions
  • Early Intervention: Allows for proactive medical management
  • Risk Assessment: Helps determine recurrence risks for future pregnancies
  • Personalized Care: Facilitates tailored medical approaches
  • Peace of Mind: Reduces uncertainty for concerned families

Understanding Your Test Results

Our genetic counseling team provides comprehensive interpretation of your results:

  • Positive Result: Indicates presence of pathogenic TSPYL1 mutation requiring specialized medical follow-up
  • Negative Result: Suggests absence of tested mutations but doesn’t rule out other genetic causes
  • Variant of Uncertain Significance: Requires additional family studies and clinical correlation
  • Carrier Status: Identifies individuals who may pass the condition to offspring

Test Information and Pricing

Test Component Details
Test Name TSPYL1 Gene Sudden Infant Death with Dysgenesis of the Testes Syndrome 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)

Pre-Test Requirements

Before scheduling your test, please ensure:

  • Complete clinical history documentation
  • Genetic counseling session to create family pedigree chart
  • Discussion of testing implications with healthcare provider
  • Understanding of potential outcomes and next steps

Nationwide Testing Availability

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, Austin, Jacksonville, Fort Worth, Columbus, Charlotte, San Francisco, Indianapolis, Seattle, Denver, Washington DC, Boston, El Paso, Nashville, Detroit, Oklahoma City, Portland, Las Vegas, Memphis, Louisville, Baltimore, and Milwaukee.

Take Action Today

Don’t let uncertainty about genetic risks affect your family’s future. Our expert genetic counselors and advanced NGS technology provide the answers you need for informed healthcare decisions. Schedule your consultation and testing today to gain clarity and peace of mind.

Call or WhatsApp us now at +1(267) 388-9828 to book your TSPYL1 genetic test and take the first step toward understanding your genetic health.