6 mL blood sample | Or Saliva Collection (In Clinic only) | USA laboratory | Results in 3 to 4 weeks
Thalassemia A and B/Fragile X syndrome/Intellectual retardation and autism/Deaf/Myelogenous muscular atrophy/Cystic fibrosis/Pompe disease
To let you know the risk of genetic inheritance that may cause certain diseases in your baby
If both of you and your partner are not a carrier, your child likely not be inherit the disease
If you are the carrier but your partner is not (or vice versa), your child likely not be inherit the disease
If both of you and your partner are carriers, your child will have 25% of chance inherited with the disease
Although this genetics test can help you understand more about your health history and your chance of having a healthy pregnancy and baby, the result is not absolute
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5 mL blood sample | USA laboratory | Results in 2-4 weeks | Conducted in Mong Kok or Wan Chai centre
Breast and gynecology (breast, ovarian, uterine)
Gastrointestinal (colorectal, gastric, pancreatic)
Endocrine (thyroid, parathyroid, pituitary)
Genitourinary (renal/urinary tract, prostate)
Skin (melanoma, basal cell carcinoma)
Brain/nervous system
Positive result = higher risk of having cancer in later stages
Genetic testing can help treatment decisions
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5 mL blood sample | Results in 2-4 weeks | Conducted in Mong Kok or Wan Chai centre
According to the statistics from Hong Kong Cancer Registry under Hospital Authority (HA) in 2021, there were over 35000 new cancer cases in Hong Kong in 2019, meaning that 96 people were diagnosed of cancer per day.
Brca gene testing is performed to predict the risk of breast cancer and ovarian cancer. Mutations in the Brca gene increase the risk of breast cancer or ovarian cancer.
What does a genetic test tell you?
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Current pre-pregnancy checkups often focus on fertility only. The bigger question is whether a couple may carry hereditary genes that could affect the child.
Planning for hereditary disease risk can be even more important.
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Saliva test | No food for 30 minutes | European laboratory | Results in 3 to 4 weeks
Rodinia is a screening test for gene variants associated with infertility. This test is suitable for...
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3 mL blood sample | USA laboratory | Results in 3 to 4 weeks | Conducted in Mong Kok or Wan Chai centre
This panel analyzes genes associated with developmental delay, intellectual disability, autism, and related conditions. Combined with clinical findings, it can help doctors confirm diagnosis, assess prognosis and progression, support early symptom detection, and provide information for family planning and genetic counseling.
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10 mL blood sample| about 6 to 8 weeks for report| Conducted in Mong Kok or Wan Chai centre
Whole genome sequencing is an advanced genetic testing technology that reads the complete genome and analyzes related hereditary information. Mutation data can be used to evaluate disease-related genes and support personalized medical planning.
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10 mL blood sample| about 4 weeks for report| Conducted in Mong Kok or Wan Chai centre| includes nutritionist consultation
Telomeres are an objective indicator of biological age. They play a critical role in cellular aging and are considered one of the key factors related to human longevity. Telomere research has also received Nobel-level recognition in health and longevity science.
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Before you decide to proceed with genetic testing, we want you to have an understanding of the possible test result you may receive. You are advice to discuss with your doctors before you decided to proceed the genetic tests ... more
G6PD deficiency is a relatively common hereditary condition in Hong Kong, affecting about 50 in 1,000 male newborns and 4 in 1,000 female newborns.
MoreWhen planning pregnancy, recessive hereditary disease genes may increase rare disease risk for the next generation and should be assessed early.
MoreA 5 mL blood-based cancer gene test may support earlier detection and treatment planning, especially for people with family cancer risk.
MoreDevelopmental delay and autism may be associated with inherited conditions. Hereditary gene testing can support earlier treatment and planning.
MoreIf cancer runs in your family, genetic testing may help clarify hereditary risk across multiple organ systems.
MorePre-pregnancy hereditary screening helps couples assess recessive gene risks before conception, not just fertility factors.
MoreUV exposure and hereditary risk both matter. Early skin cancer risk assessment can help with timely prevention and follow-up.
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