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Endocrine Cancer Gene Panel

Original price was: $1,200.Current price is: $900.

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The Endocrine Cancer Gene Panel is a comprehensive genetic screening test that analyzes multiple genes associated with hereditary endocrine cancers. This advanced Next-Generation Sequencing (NGS) test provides crucial insights into your genetic predisposition to various endocrine malignancies including thyroid, adrenal, pancreatic, and pituitary cancers. By examining specific gene mutations, the test helps identify inherited cancer syndromes that may run in families. The panel is particularly valuable for individuals with a family history of endocrine cancers or those experiencing unexplained endocrine-related symptoms. Results are typically available within 4-6 weeks and require a simple peripheral blood sample. At only $900 USD, this test offers affordable access to cutting-edge genetic cancer risk assessment, empowering you with knowledge for proactive health management and personalized prevention strategies.

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  • ISO-Accredited Laboratory, Ensuring Highest Standards
  • Trusted by Hospitals & Patients —Accredited Testing with Results
  • Direct Healthcare Provider Support + Comprehensive Reporting
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Endocrine Cancer Gene Panel: Comprehensive Genetic Cancer Risk Assessment

Understanding Endocrine Cancer Genetic Testing

The Endocrine Cancer Gene Panel represents a breakthrough in personalized medicine, offering comprehensive genetic screening for hereditary endocrine cancer syndromes. This advanced diagnostic tool utilizes Next-Generation Sequencing (NGS) technology to analyze multiple genes simultaneously, providing unprecedented insights into your genetic cancer risk profile. Endocrine cancers affect hormone-producing glands throughout the body, and many of these malignancies have strong hereditary components that can be identified through genetic testing.

What Does the Endocrine Cancer Gene Panel Measure?

This comprehensive genetic panel analyzes multiple genes associated with hereditary endocrine cancer syndromes, including:

  • RET gene mutations linked to Multiple Endocrine Neoplasia type 2
  • MEN1 gene variations associated with Multiple Endocrine Neoplasia type 1
  • VHL gene mutations connected to Von Hippel-Lindau syndrome
  • SDH complex genes related to paraganglioma and pheochromocytoma
  • TP53 gene variations associated with Li-Fraumeni syndrome
  • Additional genes implicated in thyroid, adrenal, pancreatic, and pituitary cancers

Who Should Consider Endocrine Cancer Genetic Testing?

This test is particularly recommended for individuals with:

  • Personal history of endocrine cancer diagnosed at a young age
  • Family history of multiple endocrine tumors or cancers
  • Relatives with known hereditary cancer syndrome mutations
  • Unexplained endocrine symptoms or hormone imbalances
  • Multiple primary cancers in the same individual
  • Bilateral endocrine tumors or multifocal disease
  • Rare endocrine tumors or unusual tumor presentations

Clinical Symptoms and Indicators

Consider genetic testing if you experience:

  • Unexplained thyroid nodules or growths
  • Adrenal mass discoveries on imaging studies
  • Pancreatic neuroendocrine tumors
  • Pituitary gland abnormalities
  • Multiple endocrine-related health issues
  • Early-onset endocrine cancers in family members

Benefits of Endocrine Cancer Genetic Testing

Undergoing the Endocrine Cancer Gene Panel offers numerous advantages:

  • Early Risk Identification: Detect genetic mutations before cancer develops
  • Personalized Screening: Tailor surveillance protocols based on genetic risk
  • Family Planning: Make informed decisions about genetic inheritance
  • Treatment Guidance: Inform surgical and therapeutic approaches
  • Peace of Mind: Reduce uncertainty about hereditary cancer risk
  • Proactive Health Management: Implement preventive measures early

Understanding Your Test Results

Your genetic test results will fall into one of several categories:

  • Positive Result: A known disease-causing mutation was identified, indicating increased cancer risk
  • Negative Result: No mutations detected in the genes analyzed
  • Variant of Uncertain Significance (VUS): A genetic change with unknown clinical significance
  • Benign Variant: A genetic change not associated with increased cancer risk

All results are accompanied by comprehensive genetic counseling to ensure proper interpretation and appropriate next steps. Our genetic specialists will guide you through understanding your results and developing a personalized management plan.

Test Pricing and Details

Test Component Details
Test Name Endocrine Cancer Gene Panel
Discount Price $900 USD
Regular Price $1,200 USD
Turnaround Time 4-6 weeks
Sample Type Peripheral Blood
Test Components EDTA Vacutainer (3 ml)
Testing Method Next-Generation Sequencing (NGS)

Pre-Test Requirements

The Endocrine Cancer Gene Panel requires a doctor’s prescription for testing. Please note that prescriptions are not applicable for surgery and pregnancy cases or individuals planning to travel abroad. Our team can assist with connecting you to healthcare providers who can facilitate the prescription process if needed.

Nationwide Testing Availability

We have testing facilities conveniently located across the United States, serving 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 collection centers ensures accessible testing regardless of your location.

Take Control of Your Genetic Health Today

Don’t wait to understand your genetic cancer risk. The Endocrine Cancer Gene Panel provides valuable insights that can guide your healthcare decisions and potentially save lives through early detection and prevention strategies. Our team of genetic counselors and healthcare professionals are ready to support you throughout the testing process.

Ready to schedule your Endocrine Cancer Gene Panel? Call us today at +1(267) 388-9828 or book your appointment online. Take the first step toward proactive cancer risk management and personalized healthcare planning.