Medical Genetics

Overview

The Department of Medical Genetics at Baby Memorial Hospitals focuses on understanding how genetic factors influence health, disease, and long-term well-being. The department supports patients across all age groups by identifying inherited conditions, guiding clinical decisions, and helping families understand potential health risks through structured genetic evaluation and counselling.

Services are designed to assist in early detection and risk assessment for a wide range of conditions, including developmental disorders in children, unexplained neurological symptoms, and genetic causes of infertility or pregnancy-related concerns. The department also supports prenatal care through appropriate screening and guidance, helping expectant families make informed decisions during pregnancy.

A strong emphasis is placed on preventive care, including carrier screening for inherited disorders and genetic risk evaluation for conditions that may run in families, such as certain cancers. By working closely with multiple clinical specialties, the department contributes to personalised care planning, ensuring that patients receive treatment approaches aligned with their genetic profile.

With a patient-focused approach, the Medical Genetics team provides ongoing guidance, family counselling, and long-term support, helping individuals better understand their condition and make informed healthcare choices at every stage of life.