No. PinkCare assesses inherited genetic susceptibility. It cannot determine whether cancer is currently present and is not a diagnostic cancer test.
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Discover MEDLATEC PinkCare, a women's hereditary cancer genetic test assessing inherited susceptibility to breast, ovarian and colorectal cancers through a 10-gene panel.

Est. duration | 0 - 1 hours |
Stay required | 1 - 1 days |
Recovery period | 0 - 0 weeks |
PinkCare is a hereditary cancer genetic risk assessment offered by MEDLATEC, designed to identify inherited genetic variants associated with susceptibility to certain cancers.
The test analyses a panel of 10 genes associated with hereditary cancer risk, focusing on breast, ovarian and colorectal cancers.
Unlike tests that screen for cancer-associated signals in the blood, PinkCare evaluates inherited genetic susceptibility. It does not determine whether cancer is currently present.
Breast Cancer
Assessment of inherited genetic variants associated with an increased susceptibility to breast cancer.
Ovarian Cancer
Analysis of genetic variants that may be associated with hereditary ovarian cancer risk.
Colorectal Cancer
Evaluation of inherited genetic factors associated with susceptibility to certain forms of colorectal cancer.
Personalised Hereditary Cancer Risk Assessment
PinkCare provides information about inherited genetic factors that may influence an individual's susceptibility to selected cancers.
Focused 10-Gene Panel
The test analyses 10 genes associated with hereditary cancer risk, focusing on breast, ovarian and colorectal cancers.
Supports Preventive Healthcare Planning
Results may help patients and healthcare professionals discuss appropriate screening strategies, further genetic assessment and personalised healthcare planning.
Provides Information Relevant to Family Health
Some inherited genetic findings may have implications for biological relatives. Genetic counselling can help patients understand whether additional family risk assessment is appropriate.
Generally a One-Time Genetic Assessment
Inherited genetic variants are generally stable throughout life. Routine annual repetition of the same germline genetic test is therefore usually unnecessary, although additional testing may be appropriate as medical knowledge or individual circumstances change.
PinkCare may be considered by individuals who:
Have a family history of breast, ovarian or colorectal cancer.
Have relatives diagnosed with cancer at a relatively young age.
Have multiple biological relatives affected by related cancers.
Have a personal history that raises concern about hereditary cancer susceptibility.
Have been advised by a healthcare professional to consider genetic testing.
Want to understand inherited cancer risk as part of a preventive healthcare plan.
The suitability of genetic testing should be assessed based on individual medical history, family history and professional guidance.
Pre-Test Consultation: Review medical history, family cancer history and genetic testing suitability.
Sample Collection: A biological sample is collected according to MEDLATEC's laboratory requirements.
Genetic Analysis: The laboratory examines the selected 10-gene panel for relevant genetic variants.
Results: Results are generally expected in approximately 15 working days, subject to laboratory confirmation.
Genetic Counselling and Follow-Up: A qualified healthcare professional may explain the findings and recommend 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 contribute to an individual's overall risk.
Variant of Uncertain Significance (VUS)
Some genetic changes cannot currently be classified as harmful or harmless. These findings generally should not independently determine clinical management.
Test Name: PinkCare
Test Category: Hereditary Cancer Genetic Risk Assessment
Genetic Panel: 10 Genes
Cancer Risks Assessed: Breast, Ovarian and Colorectal 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 PinkCare appointment with MEDLATEC, provide pre-arrival guidance and assist with travel and follow-up arrangements.
PinkCare is a hereditary genetic risk assessment, not a test for diagnosing cancer or detecting an existing tumour.
An increased genetic risk does not mean cancer will necessarily develop, and a negative result does not eliminate cancer risk.
Genetic testing results should be interpreted by qualified healthcare professionals, ideally with access to genetic counselling. Recommended cancer screening and clinical assessment may still be necessary regardless of the genetic test result.
Top experts performing this treatment
No. PinkCare assesses inherited genetic susceptibility. It cannot determine whether cancer is currently present and is not a diagnostic cancer test.
PinkCare focuses on hereditary susceptibility to breast, ovarian and colorectal 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.
Inherited genetic variants are generally stable throughout life, so routine annual repetition of the same germline test is usually unnecessary. Further testing may be appropriate if clinical recommendations change.
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