Introducing genetic testing with case finding for familial hypercholesterolaemia in primary care: qualitative study of patient and health professional experience

Abstract excerpt

BACKGROUND: Familial hypercholesterolaemia (FH) is a common inherited condition causing elevated cholesterol, premature heart disease, and early death. Although FH can be effectively treated, over 80% of people with FH remain undetected. AIM: To explore patient and health professional experiences of introducing genetic testing with case finding for FH in primary care. DESIGN AND SETTING: Qualitative study in UK...

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