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Examinations
- Essential 50-Gene Expanded Panel (ENCODE)
Terms and Conditions
- All packages are inclusive of doctor’s fee, medical supplies, and hospital and nursing services fee.
- Expenses for additional consultation, investigation, or treatment other than the package are not included.
- All packages are transferable
- Please make an appointment at least 2 days prior to using the services via BNH Cares at LINE @BNHhospital or contact our staff for assistance at LINE @Mbrace
- Services are available at the Women’s Health Centre, 4th floor, zone A, BNH Hospital. Monday – Sunday at 7 am. – 7 pm.
- For more information, please contact the Women’s Health Centre, BNH Hospital at 02-022-0788 and 02-022-0850
Preparation
- No fasting is required before the test.
“Do you carry genes that increase your risk of hereditary cancer?”
If you wish to know whether you carry genetic variants that increase your risk of developing cancer in the future, hereditary gene testing can evaluate your lifetime risk.
- Ideal for risk assessment prior to the onset of disease.
- If a gene mutation is detected, prevention and monitoring plans can be established early.
- Provides insight into potential risks that could be passed down within your family.
Genetic analysis of inherited genes—such as BRCA1, BRCA2, and other cancer-related genes—helps evaluate your risk prior to the onset of breast, ovarian, and other hereditary cancers. Includes international-standard lab reports and expert medical guidance for long-term prevention, screening, and healthcare planning.
- Assessment of personal health history and family medical history
- Pre- and/or post-test Genetic Counselling
- Personalised recommendations for monitoring, screening, and prevention should a mutation be found
Your DNA remains unchanged throughout your lifetime, so testing is required only once (unless medically indicated otherwise).
Which hereditary cancers can be evaluated?
Helps assess the risk of inherited cancers across key major types, including:
Common Cancers:
- Breast Cancer
- Ovarian Cancer
- Fallopian Tube Cancer
- Primary Peritoneal Cancer
- Colorectal Cancer
- Endometrial Cancer
Gastrointestinal Cancers:
- Stomach Cancer
- Pancreatic Cancer
Cancers in Men:
- Prostate Cancer
- Male Breast Cancer
Other Gene-Related Cancers:
- Thyroid Cancer
- Kidney Cancer
- Melanoma (Skin Cancer)
- Neuroendocrine Tumours
- Pheochromocytoma and Paraganglioma
Who is hereditary gene testing suitable for?
1. Individuals with a family history of cancer, particularly involving parents, siblings, or close relatives who:
- Developed cancer at a young age
- Had multiple family members diagnosed with the same type of cancer
- Were diagnosed with multiple types of cancer in a single person
- Had cancers associated with hereditary genetics (e.g. breast, ovarian, colorectal, endometrial, pancreatic, or prostate cancer)
2. Individuals with a personal history of cancer, such as:
- Diagnosis at an earlier age than typically observed
- Having more than one primary cancer type
- Bilateral cancers (e.g. both breasts) or multiple recurring sites
- Male breast cancer
- Specific cancer subtypes or characteristics suspected by a doctor to be hereditary
3. Individuals with a family member who tested positive for a gene mutation:
- Helps determine if you have inherited the specific gene variant found in a first-degree relative.
4.Individuals with an unknown family health history:
- E.g. adopted individuals or those with incomplete family records. A pre-test evaluation by a specialist is advised to select the most appropriate panel.
5.Individuals seeking long-term preventive healthcare planning:
- Suitable for those wishing to understand their genetic risk profile to inform lifelong screening and health strategies.
When should you consult a doctor before deciding to test?
- No personal or family history suggesting cancer risk:
Testing can be performed, but the likelihood of finding a clinically actionable variant is lower, and findings of uncertain significance may occur. Consulting a physician beforehand helps weigh the benefits and limitations. - Seeking to confirm a current cancer diagnosis:
This test is not a diagnostic tool for active cancer and cannot replace routine check-ups, diagnostic imaging, or biopsies. - Unaffected relatives of a cancer patient:
Doctors generally recommend testing an affected family member first, as it yields clearer genetic insights. Unaffected relatives can then be tested specifically for any identified mutation. - Children or minors:
Testing children for adult-onset hereditary cancer risks requires careful consideration due to psychological and ethical impacts. It is usually deferred until the individual can give informed consent as an adult, unless medical management begins in childhood. - Individuals unprepared for potential emotional impacts:
Results can affect emotions, family planning, and broader family dynamics. Pre-test counseling helps ensure you are fully prepared for possible outcomes.
Key Takeaways
- Positive Result (+): Indicates an increased risk, but does not mean you will definitely develop cancer.
- Negative Result (-): Does not mean you have zero risk of developing cancer.
- Variant of Uncertain Significance: Some individuals may receive results showing genetic variations whose medical implications are not yet fully understood.
- Genetic results do not replace age-appropriate cancer screenings or standard medical advice.
- Medical consultation before and after the test is strongly recommended.
Frequently Asked Questions (FAQ) about Genetic Cancer Testing 90 Genes
Q: Who is the 90-gene cancer test suitable for? A: It suits those with a family history of cancer or who want a comprehensive hereditary cancer risk assessment across 90 genes in a single test.
Q: How should I prepare? A: It uses a blood sample with no fasting required; bring your family cancer history to aid interpretation.
Q: How long does it take and what does the result tell me? A: Results are available within a few weeks and show risk for multiple cancers based on the detected genes, for proactive surveillance and prevention.
Q: Is genetic counseling or consultation available? A: Yes. Physicians and specialists are available to explain your results and next steps. You can book an appointment at BNH Hospital via the website or by phone.
Other Genomic (DNA) Screening Packages You May Be Interested In
A: It suits those with a family history of cancer or who want a comprehensive hereditary cancer risk assessment across 90 genes in a single test.
A: It uses a blood sample with no fasting required; bring your family cancer history to aid interpretation.
A: Results are available within a few weeks and show risk for multiple cancers based on the detected genes, for proactive surveillance and prevention.
A: Yes. Physicians and specialists are available to explain your results and next steps. You can book an appointment at BNH Hospital via the website or by phone.
