A genetic condition identified in a family member: clinical guidance for GPs

In many cases, GPs are the first point of contact when patients receive concerning health information.  This is particularly true for genetic conditions - when a patient finds out that a family member has been diagnosed with something which may run in the family, patients will often turn to their GP for guidance about their own health and next steps.

While referral to a specialist is often appropriate, GPs play a crucial role in supporting patients and families through this journey. This interactive eLearning module uses real-world case studies to provide practical, GP-focused guidance on genetic conditions. You will learn when genetic testing is warranted, which genetic and genomic tests you can order, how to interpret and communicate test results effectively, and how to support patients and their relatives in the context of inherited risk. The module also clarifies your role within the broader clinical landscape, including referral pathways, genetic counselling, and psychosocial support.

This is a Medcast Continuing Medical Education (CME) course.