Genetic Familial Hypercholesterolaemia

Familial Hypercholesterolaemia (FH) is a common inherited condition that affects around 1 in 250 people in the UK, causing significantly elevated cholesterol levels from a young age.

If left undiagnosed and untreated, FH can lead to premature heart disease. However, with early detection, it can be effectively managed through lifestyle changes and medication.

Genetic testing for FH helps confirm a diagnosis, assess family risk, and support proactive heart health management for the long term.