A Family History of Hypercholesterolemia - the Role of Genetics Abstract. Genetic testing is rarely used in Switzerland to confirm the clinical diagnosis of familial hypercholesterolemia. However, cascade genetic testing from an index case is recommended by the guidelines. By describing a patient and his family with severe hypercholesterolemia, we discuss the benefits, risks and barriers regarding the implementation of genetics for familial hypercholesterolemia. Family screening with genetic testing could become a standard of care for severe hypercholesterolemia
Familial hypercholesterolemia (FH) is an autosomal dominant disorder characterized by abnormally hig...
This editorial refers to ‘Diagnosing familial hypercho-lesterolemia: the relevance of genetic testin...
AIMS: Familial hypercholesterolaemia (FH) is an autosomal dominant disease that warrants early diagn...
Familial hypercholesterolemia (FH) is a genetic disorder associated with an increased risk of early-...
International audiencePurpose of review We provide an overview of molecular diagnosis for familial h...
Background and Aims: The large-scale implementation and effectiveness of genetic cascade screening f...
Abstract Familial Hypercholesterolemia (FH) is a common cause of premature cardiovascular disease an...
Familial hypercholesterolemia (FH) is a genetic disorder of cholesterol metabolism caused by mutatio...
Although awareness of familial hypercholesterolemia (FH) is increasing, this common, potentially fat...
Introduction: Familial hypercholesterolemia (FH) is a highly prevalent condition, predisposing indiv...
International audienceFamilial hypercholesterolemia (FH) is caused by mutations in LDLR (low-density...
Although awareness of familial hypercholesterolemia (FH) is increasing, this common, potentially fat...
This paper considers the implications of genetic testing in the case of familial hypercholesterolaem...
AIMS: We assembled a cohort of patients with familial hypercholesterolaemia (FH) for both basic and ...
AIMS: We assembled a cohort of patients with familial hypercholesterolaemia (FH) for both basic and ...
Familial hypercholesterolemia (FH) is an autosomal dominant disorder characterized by abnormally hig...
This editorial refers to ‘Diagnosing familial hypercho-lesterolemia: the relevance of genetic testin...
AIMS: Familial hypercholesterolaemia (FH) is an autosomal dominant disease that warrants early diagn...
Familial hypercholesterolemia (FH) is a genetic disorder associated with an increased risk of early-...
International audiencePurpose of review We provide an overview of molecular diagnosis for familial h...
Background and Aims: The large-scale implementation and effectiveness of genetic cascade screening f...
Abstract Familial Hypercholesterolemia (FH) is a common cause of premature cardiovascular disease an...
Familial hypercholesterolemia (FH) is a genetic disorder of cholesterol metabolism caused by mutatio...
Although awareness of familial hypercholesterolemia (FH) is increasing, this common, potentially fat...
Introduction: Familial hypercholesterolemia (FH) is a highly prevalent condition, predisposing indiv...
International audienceFamilial hypercholesterolemia (FH) is caused by mutations in LDLR (low-density...
Although awareness of familial hypercholesterolemia (FH) is increasing, this common, potentially fat...
This paper considers the implications of genetic testing in the case of familial hypercholesterolaem...
AIMS: We assembled a cohort of patients with familial hypercholesterolaemia (FH) for both basic and ...
AIMS: We assembled a cohort of patients with familial hypercholesterolaemia (FH) for both basic and ...
Familial hypercholesterolemia (FH) is an autosomal dominant disorder characterized by abnormally hig...
This editorial refers to ‘Diagnosing familial hypercho-lesterolemia: the relevance of genetic testin...
AIMS: Familial hypercholesterolaemia (FH) is an autosomal dominant disease that warrants early diagn...