Familial hypercholesterolaemia is the most commonly encountered genetic condition that
predisposes individuals to premature cardiovascular disease. Nevertheless, most patients …

Familial hypercholesterolaemia is a common inherited disorder characterized by abnormally
elevated serum levels of low-density lipoprotein (LDL) cholesterol from birth, which in time …

Optimal care for familial hypercholesterolaemia (FH) requires patient-centred management,
multidisciplinary teamwork, involvement of primary care practitioners, patient networks …

Objective: Familial hypercholesterolemia (FH) is associated with a high risk of premature
atherosclerotic cardiovascular disease (ASCVD). However, this risk is highly heterogeneous …

Familial hypercholesterolemia (FH) is the most common monogenic disorder causing
premature atherosclerotic cardiovascular disease. It affects 1 in 250 individuals worldwide …

Familial hypercholesterolaemia (FH) is a common autosomal semi-dominant and highly
penetrant disorder of the low-density lipoprotein (LDL) receptor pathway, characterised by …

Background Current data from individual studies present conflicting evidence about the
relationship between risk factors and cardiovascular disease (CVD) in heterozygous familial …

Familial hypercholesterolemia (FH) is a genetic disease characterized by high low-density
lipoprotein (LDL) cholesterol (LDL-c) concentrations that increase cardiovascular risk and …

Familial hypercholesterolaemia (FH) is a genetic disorder affecting the metabolism of low-
density lipoprotein (LDL) particles, leading to high LDL-cholesterol levels maintained over …

Financial declaration A-Economically relevant payments of any kind made to (i) you,(ii) your
spouse/partner or any other person living with you,(iii) any legal person in which any of …