Familial hypercholesterolemia (FH) is a frequently undiagnosed genetic disease characterized by substantial elevations of low-density lipoprotein cholesterol (LDL-C). The prevalence of heterozygous FH (HeFH) in the general population is 1:500 inhabitants, while the prevalence of homozygous FH (HoFH) is 1:1,000,000. If FH is not identified and aggressively treated at an early age, affected individuals have a 20-fold increased lifetime risk of coronary heart disease compared with the general population. This narrative review provide a concise overview of recommendations for diagnosis and treatment of adults and children with FH, and discuss the utility of considering FH as a comorbidity at the entry of cardiac rehabilitation programme
Familial hypercholesterolaemia (FH) is a dominantly inherited disorder present from birth that marke...
Familial hypercholesterolemia (FH) is a genetic disorder resulting from mutations in genes encoding ...
Familial hypercholesterolemia (FH) is an autosomal codominant genetic disorder of lipoprotein metabo...
Familial hypercholesterolemia (FH) is a frequently undiagnosed genetic disease characterized by subs...
Familial hypercholesterolaemia (FH) is a dominantly inherited disorder present from birth that marke...
Background and aims Familial hypercholesterolemia (FH) is a genetic disorder characterized by high l...
Familial hypercholesterolaemia (FH) is a dominantly inherited disorder present from birth that marke...
Familial hypercholesterolaemia (FH) is the main genetic cause of premature coronary heart disease (...
Familial hypercholesterolaemia (FH) is a genetic disorder affecting the metabolism of low-density li...
Familial hypercholesterolemia (FH) is a common genetic cause of premature cardiovascular disease (CV...
Familial Hypercholesterolaemia (FH) is the commonest autosomal co-dominantly inherited condition af...
Familial hypercholesterolemia (FH) is a common genetic cause of premature cardiovascular disease (CV...
This review article assesses the clinical features, diagnosis and management of familial hypercholes...
This review article assesses the clinical fea-tures, diagnosis and management of familial hyperchole...
Familial hypercholesterolemia (FH) is a dominantly inherited disorder present from birth that marked...
Familial hypercholesterolaemia (FH) is a dominantly inherited disorder present from birth that marke...
Familial hypercholesterolemia (FH) is a genetic disorder resulting from mutations in genes encoding ...
Familial hypercholesterolemia (FH) is an autosomal codominant genetic disorder of lipoprotein metabo...
Familial hypercholesterolemia (FH) is a frequently undiagnosed genetic disease characterized by subs...
Familial hypercholesterolaemia (FH) is a dominantly inherited disorder present from birth that marke...
Background and aims Familial hypercholesterolemia (FH) is a genetic disorder characterized by high l...
Familial hypercholesterolaemia (FH) is a dominantly inherited disorder present from birth that marke...
Familial hypercholesterolaemia (FH) is the main genetic cause of premature coronary heart disease (...
Familial hypercholesterolaemia (FH) is a genetic disorder affecting the metabolism of low-density li...
Familial hypercholesterolemia (FH) is a common genetic cause of premature cardiovascular disease (CV...
Familial Hypercholesterolaemia (FH) is the commonest autosomal co-dominantly inherited condition af...
Familial hypercholesterolemia (FH) is a common genetic cause of premature cardiovascular disease (CV...
This review article assesses the clinical features, diagnosis and management of familial hypercholes...
This review article assesses the clinical fea-tures, diagnosis and management of familial hyperchole...
Familial hypercholesterolemia (FH) is a dominantly inherited disorder present from birth that marked...
Familial hypercholesterolaemia (FH) is a dominantly inherited disorder present from birth that marke...
Familial hypercholesterolemia (FH) is a genetic disorder resulting from mutations in genes encoding ...
Familial hypercholesterolemia (FH) is an autosomal codominant genetic disorder of lipoprotein metabo...