We provide professional clinical assessment, genetic diagnosis, genetic counseling and support services to individuals and families affected by genetic diseases or at risk. Help you make informed health decisions with expertise in genetics and genomics.
Service objects
Children and adults:
Suspected genetic diseases (such as birth defects, autism, developmental delays, growth disorders, metabolic diseases, neurodegenerative diseases, etc.)
Families with high risk of cancer:
Evaluation and testing of hereditary cancers (such as breast cancer, ovarian cancer, colon cancer)
Couples planning for marriage/birth:
Gene carrier screening and assessment of recurrent miscarriage
Abnormal prenatal examination of pregnant women:
Interpretation of prenatal screening/test results
Persons with unknown symptoms:
Genetic diagnosis of difficult diseases
Family history of genetic diseases:
Gene testing for hereditary diseases
Core Services
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Comprehensive genetic counseling
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Genetic risk assessment
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Analysis of disease diagnosis, genetic patterns and treatment plans
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Psychological and emotional support
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Family communication guidance
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Advanced genetic testing
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Cutting-edge testing technology (chromosome/gene/genome testing)
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Professional interpretation of complex reports
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Pre/post-test counseling
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Personalized medical coordination
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Specialty referral (cardiology, neurology, etc.)
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Long-term monitoring plan
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Resource linking between support organizations and patient groups
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Medical treatment process
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Preparation before diagnosis
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Carry medical records, genetic reports and family medical history
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Face-to-face consultation
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Discussing health concerns
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Family medical history analysis
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Clinical evaluation (including physical examination, if necessary)
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Personalized risk assessment
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Detection decision
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Clearly explain testing options, fees and restrictions
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Respect independent choices, no mandatory testing*
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Follow-up
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Interpretation of face-to-face results
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Provide a written summary for you and the treating physician
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Ongoing support services
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Service Commitment
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Privacy protection: Strictly protect your privacy
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Equality principle: no discrimination based on genes, race or background
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Informed Consent: Written consent is required for all genetic testing
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Family-oriented: Pay attention to the impact of disease on the entire family
Medical treatment guidelines
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Referral requirements: A physician referral letter is recommended but not mandatory
* Fee description: Most medical insurances are accepted and self-pay services are provided
Preparation checklist
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Compile the medical history and medical records of relatives
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List your questions and concerns
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Bring photos of sick relatives (if any) to assist assessment




吳瑞芬醫生
劉家輝醫生