Although awareness of familial hypercholesterolemia (FH) is increasing, this common,
potentially fatal, treatable condition remains underdiagnosed. Despite FH being a genetic …

Familial hypercholesterolaemia (FH) is a common genetic cause of premature coronary
heart disease (CHD). Globally, one baby is born with FH every minute. If diagnosed and …

Familial hypercholesterolaemia (FH) is a dominantly inherited disorder present from birth
that markedly elevates plasma low-density lipoprotein (LDL) cholesterol and causes …

Disorders of lipid metabolism. Clinical Guidelines 2023 | Ezhov | Russian Journal of
Cardiology Russian Journal of Cardiology eng | рус User ISSN 1560-4071 (Print) ISSN …

При участии: Национального общества по изучению атеросклероза (НОА), Российской
ассоциации эндокринологов (РАЭ), Российского общества кардиосоматической …

Background Familial hypercholesterolemia is one of the most common inherited metabolic
diseases and is an autosomal dominant disorder meaning heterozygotes, or carriers, are …

Background and Aims: Familial hypercholesterolemia (FH) is one of the major risk factor for
the progression of atherosclerosis and coronary artery disease. This study focused on …

There is compelling evidence that the elevated plasma lipoprotein (a)[Lp (a)] levels increase
the risk of atherosclerotic cardiovascular disease (ASCVD) in the general population. Like …

Importance Elevations in levels of total, low-density lipoprotein, and non–high-density
lipoprotein cholesterol; lower levels of high-density lipoprotein cholesterol; and, to a lesser …

Familial hypercholesterolemia (FH) is a dominantly inherited disorder present from birth that
markedly elevates plasma low-density lipoprotein cholesterol and causes premature …