No. MenCare assesses inherited genetic susceptibility. It cannot determine whether cancer is currently present and is not a diagnostic cancer test.
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Explore MEDLATEC MenCare, a genetic test that assesses inherited susceptibility to prostate, colorectal and stomach cancers through the analysis of 10 genes.

Est. duration | 0 - 1 hours |
Stay required | 1 - 1 days |
Recovery period | 0 - 0 weeks |
MenCare is a hereditary cancer genetic risk assessment offered by MEDLATEC, designed to identify inherited genetic variants associated with increased susceptibility to certain cancers in men.
The test analyses a panel of 10 genes associated with hereditary cancer risk, focusing on prostate, colorectal and stomach cancers.
Unlike blood-based cancer signal screening tests, MenCare evaluates inherited cancer susceptibility. It does not detect whether cancer is currently present.
Prostate Cancer
Assessment of inherited genetic variants associated with susceptibility to prostate cancer.
Colorectal Cancer
Analysis of genetic variants that may be associated with hereditary colorectal cancer risk.
Stomach Cancer
Evaluation of genetic variants associated with inherited susceptibility to certain forms of stomach cancer.
Personalised Genetic Risk Assessment
MenCare provides information about inherited genetic factors that may influence susceptibility to selected cancers.
Focused 10-Gene Panel
The test examines 10 genes associated with hereditary cancer risk, focusing on cancers relevant to men's health.
Supports Preventive Healthcare Planning
Results may help patients and healthcare professionals discuss personalised screening strategies, lifestyle considerations and further genetic evaluation where appropriate.
Useful for Family Health Discussions
Certain inherited genetic findings may have implications for biological relatives. Genetic counselling can help patients understand whether family members should consider additional assessment.
Generally a One-Time Genetic Assessment
Because inherited DNA variants are generally stable throughout life, germline genetic testing typically does not require routine annual repetition. Additional testing may be appropriate if genetic knowledge or clinical circumstances change.
MenCare may be considered by individuals who:
Have a personal or family history of prostate, colorectal or stomach cancer.
Have relatives diagnosed with cancer at a relatively young age.
Have multiple relatives affected by related cancer types.
Want to discuss hereditary cancer risk with a qualified healthcare professional.
Have been advised to undergo genetic risk assessment.
The decision to undergo testing should be guided by individual medical and family history. A focused 10-gene panel may not cover every hereditary cancer syndrome.
Pre-Test Consultation: Review personal medical history, family cancer history and genetic testing suitability.
Sample Collection: A biological sample is collected according to MEDLATEC's testing requirements.
Genetic Analysis: The laboratory analyses the selected 10-gene panel.
Results: Results are generally expected in approximately 15 working days, subject to laboratory confirmation.
Genetic Counselling and Follow-Up: A qualified professional may explain the findings and discuss appropriate next steps.
Pathogenic or Likely Pathogenic Variant
A clinically significant inherited genetic variant may indicate increased susceptibility to certain cancers. It does not mean that cancer is currently present or will definitely develop.
No Reportable Pathogenic Variant Identified
A negative result does not eliminate hereditary or non-hereditary cancer risk. Other genetic factors, family history and environmental influences may still be relevant.
Variant of Uncertain Significance (VUS)
Some genetic changes cannot currently be classified as harmful or harmless. Such findings generally should not independently determine medical management.
Test Name: MenCare
Test Category: Hereditary Cancer Genetic Risk Assessment
Genetic Panel: 10 Genes
Cancer Risks Assessed: Prostate, Colorectal and Stomach Cancers
Purpose: Assessment of Inherited Cancer Susceptibility
Expected Result Time: Approximately 15 Working Days
MediHub supports international patients travelling to Vietnam for healthcare services, including genetic testing and preventive healthcare planning.
Our support services may include:
Healthcare service and genetic testing consultation
Appointment scheduling with MEDLATEC
Pre-arrival guidance and preparation
Visa and travel assistance where required
Airport transfers and local transportation
Accommodation arrangements
Medical interpreter coordination
Assistance during medical appointments
Medical results and follow-up coordination
Travel and tourism arrangements during your stay
Interested in understanding your hereditary cancer risk?
Contact MediHub for personalised assistance in planning your genetic testing journey in Vietnam. Our team can help coordinate your MenCare appointment, discuss travel arrangements and assist with follow-up planning.
MenCare is a hereditary genetic risk assessment, not a test for diagnosing cancer or detecting an existing tumour.
An increased genetic risk does not mean that cancer will necessarily develop, and a negative result does not eliminate cancer risk.
Genetic testing results should be interpreted by appropriately qualified healthcare professionals, ideally with access to genetic counselling. Routine cancer screening and clinical assessment may still be necessary.
Top experts performing this treatment
No. MenCare assesses inherited genetic susceptibility. It cannot determine whether cancer is currently present and is not a diagnostic cancer test.
The test focuses on hereditary susceptibility to prostate, colorectal and stomach cancers. It does not cover every genetic cause of these cancers.
Individuals with relevant personal or family cancer histories may benefit from discussing genetic testing with a healthcare professional. Suitability depends on individual circumstances.
Germline genetic variants are generally stable throughout life, so routine annual repetition is usually unnecessary. Further testing may be considered if clinical recommendations change.
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