Genetic Testing: Analyzes DNA to identify mutations or variations that may increase the risk of developing specific cancers or other genetic conditions. Includes tests for BRCA1/2, Lynch syndrome, and other relevant markers.
Risk Assessment: Evaluates personal and family health histories to determine the risk of hereditary cancers. Helps in creating personalized surveillance and prevention plans.
Family Planning Guidance: Offers support and options for individuals or couples considering genetic risks when planning for children.
Personalized Treatment Planning: Integrates genetic information into treatment strategies to tailor therapies that are most effective based on individual genetic profiles.
Educational Support: Provides information about genetic conditions, testing processes, and potential outcomes to help patients make informed decisions.
Genetic Clinic Services aim to empower patients with knowledge and personalized care plans, enhancing early detection, prevention, and treatment of genetic conditions.
