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Hereditary Cancer Testing

Identify genetic mutations that may increase your risk for certain cancers
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Hereditary Cancer Testing

Hereditary Cancer Testing

Hereditary Cancer Testing involves analyzing your genetic material to identify mutations that increase your risk of developing cancer. This proactive approach enables early detection and personalized management strategies to reduce cancer risk and improve outcomes.

Benefits:

  • Early Intervention: Enables early surveillance and preventive measures to reduce the risk of developing cancer or detect it at an early stage.
  • Informed Decision-Making: Provides clear information about your genetic risk, guiding decisions about lifestyle changes, screening, and preventive surgeries.
  • Family Health Awareness: Helps identify genetic risks for family members, facilitating family-wide preventive strategies and early interventions.
Hereditary_Cancer_Testing

Features:

  • Genetic Analysis: Comprehensive testing of genes associated with hereditary cancer syndromes, such as BRCA1, BRCA2, and Lynch syndrome.
  • Early Detection: Identifies genetic predispositions to cancer, allowing for early surveillance and preventive measures.
  • Personalized Risk Assessment: Provides individualized risk profiles based on genetic findings, helping tailor preventive and treatment strategies.
  • Family Implications: Offers insights into the potential genetic risks for family members, supporting informed family planning and preventive care.

Who Should Consider Hereditary Cancer Testing:

  • Family History: Individuals with a family history of cancer, especially if multiple family members or early-onset cases are involved.
  • Personal Cancer History: People with a personal history of cancer who want to understand if genetic factors may have contributed.
  • Ethnic Background: Individuals from ethnic groups with higher prevalence of certain hereditary cancer syndromes.

Frequently Asked Questions (FAQs)

What is Hereditary Cancer Testing?
It is a genetic test that identifies mutations associated with an increased risk of developing certain types of cancer.
What happens if a mutation is found?
If a genetic mutation is identified, your healthcare provider will discuss your risk management options, including increased surveillance, preventive measures, or risk-reducing surgeries.
Are there any risks associated with the test?
Hereditary cancer testing is a non-invasive procedure with no physical risks. The potential emotional impact of learning about genetic risks will be discussed with you, and support is available throughout the process.