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CYLD Gene Spiegler-Brooke Syndrome NGS Genetic DNA Test

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

-29%

The CYLD Gene Spiegler-Brooke Syndrome NGS Genetic DNA Test is a cutting-edge genetic analysis that identifies mutations in the CYLD gene, which is associated with inherited cancer predisposition syndromes. This comprehensive test utilizes Next-Generation Sequencing (NGS) technology to provide detailed insights into genetic risk factors for multiple tumor types, including skin tumors, salivary gland tumors, and other neoplasms. Individuals with a family history of multiple skin tumors, Brooke-Spiegler syndrome, or familial cylindromatosis should consider this test. The test provides crucial information for early detection, personalized screening protocols, and informed family planning decisions. Results are typically available within 3-4 weeks from sample collection. The test is priced at $500 USD with a regular price of $700 USD, making advanced genetic testing accessible to patients across the United States.

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CYLD Gene Spiegler-Brooke Syndrome NGS Genetic DNA Test

Comprehensive Genetic Testing for Inherited Cancer Syndromes

The CYLD Gene Spiegler-Brooke Syndrome NGS Genetic DNA Test represents a breakthrough in personalized medicine for individuals at risk of inherited cancer syndromes. This advanced diagnostic tool utilizes cutting-edge Next-Generation Sequencing technology to analyze the CYLD gene, which plays a critical role in tumor suppression and cellular regulation. Understanding your genetic predisposition to these conditions can significantly impact your healthcare journey and provide valuable insights for proactive health management.

What Does This Test Measure?

This comprehensive genetic analysis specifically targets the CYLD gene, which is responsible for encoding a deubiquitinating enzyme that regulates multiple cellular pathways. The test detects:

  • Pathogenic variants in the CYLD gene associated with Brooke-Spiegler syndrome
  • Mutations linked to familial cylindromatosis
  • Genetic alterations connected to multiple familial trichoepithelioma
  • Variants that increase susceptibility to various tumor types

The NGS technology employed provides high-resolution analysis of the entire coding region and critical regulatory elements of the CYLD gene, ensuring comprehensive mutation detection with exceptional accuracy.

Who Should Consider This Test?

This genetic test is particularly recommended for individuals who exhibit:

  • Personal history of multiple skin tumors, especially cylindromas or trichoepitheliomas
  • Family history of Brooke-Spiegler syndrome or related conditions
  • Development of multiple salivary gland tumors
  • Early-onset skin tumors or unusual tumor patterns
  • Concerns about inherited cancer risk in their family
  • Planning for family and wanting to understand genetic inheritance patterns

Clinical Benefits of Genetic Testing

Undergoing the CYLD gene test provides numerous advantages for your healthcare management:

  • Early Detection: Identify genetic risk factors before symptoms develop
  • Personalized Screening: Develop targeted surveillance protocols based on genetic findings
  • Family Planning: Make informed decisions about genetic inheritance and family health
  • Treatment Guidance: Inform treatment approaches and surgical planning
  • Peace of Mind: Reduce uncertainty about genetic risk factors
  • Proactive Management: Implement preventive measures and early interventions

Understanding Your Test Results

Your genetic test results will be carefully interpreted by our team of certified genetic counselors and medical geneticists. Possible outcomes include:

  • Positive Result: Identification of a pathogenic variant in the CYLD gene, indicating increased risk for associated conditions
  • Negative Result: No disease-causing variants detected, though family history remains important
  • Variant of Uncertain Significance: Identification of genetic changes with unclear clinical implications
  • Benign Variants: Common genetic variations not associated with increased disease risk

All positive results include comprehensive genetic counseling to help you understand the implications and develop an appropriate management plan.

Test Details and Pricing

Test Component Details
Test Name CYLD Gene Spiegler-Brooke Syndrome 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

Pre-Test Requirements

Before undergoing testing, patients should provide:

  • Complete clinical history relevant to CYLD-related conditions
  • Participation in a genetic counseling session
  • Development of a detailed pedigree chart documenting family members affected by CYLD-related syndromes
  • Informed consent understanding the implications of genetic testing

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. Our network of certified collection centers ensures accessible genetic testing services nationwide.

Take Control of Your Genetic Health

Understanding your genetic risk factors is the first step toward proactive health management. The CYLD Gene Spiegler-Brooke Syndrome NGS Genetic DNA Test provides valuable insights that can guide your healthcare decisions and potentially impact your family’s health for generations to come.

Ready to schedule your genetic test? Contact our genetic counseling team today at +1(267) 388-9828 or book your appointment online. Our specialists are available to answer your questions and guide you through the testing process with compassion and expertise.

Take the first step toward understanding your genetic health and making informed decisions about your future wellness. Book your CYLD gene test today and embrace the power of personalized medicine.