HOME | What does the Registry do?

Our Registry provides service for families with proven or suspected to have hereditary colon cancer syndromes. Please refer to our recruitment criteria for detail.

Record-keeping
Pedigree of affected families are formulated and updated. A database is kept for medical information and screening record of recruited family members;

Genetic-guided screening programme
Formulate and organise an individual tailored screening programme for at-risk family members using a combination of clinical and genetic methods;

Counselling
Provide genetic counselling and offer support to affected families.

Registry Information
Mission & Service Target
Referral & Entry Criteria
Registry Team Members

Areas of Work
Clinical Screening Service
Education & Training
Research & International

Registry Reports
Annual Report
Recruitment Statistics
Report on Clinical Activities
Report on Laboratory Activities

Publications

Screening
Hereditary Colorectal Cancer Screening
Screening Guidelines

FAP
HNPCC

Self-help Group
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FAP self-help group
HNPCC self-help group

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Frequently Asked Questions Index/Glossary

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