Learning About Familial Hypercholesterolemia. What is familial hypercholesterolemia? What are the symptoms of familial hypercholesterolemia? How is ...
Familial hypercholesterolemia (FH) is an autosomal dominant genetic condition characterized by very high levels of total cholesterol and low-density ...
Familial hypercholesterolemia (FH) is an autosomal dominant disorder that causes severe elevations in total cholesterol and low-density lipoprotein ...
Familial hypercholesterolemia (abbreviated FH, also spelled familial hypercholesterolaemia) is a genetic disorder characterized by high cholesterol levels ...
Familial hypercholesterolemia (FH) is an inherited condition that results in high levels of total cholesterol and LDL (low-density lipoprotein) cholesterol.
Hypercholesterolemia is a condition characterized by very high levels of cholesterol in the blood. Cholesterol is a waxy, fat-like substance that is ...
Familial hypercholesterolemia is a genetic disorder. It is caused by a defect on chromosome 19. The defect makes the body unable to remove low density ...
The FH Foundation is a patient-centered non-profit dedicated to research, advocacy, and education of all forms of familial hypercholesterolemia
Learn about the causes, symptoms, and treatment of homozygous familial hypercholesterolemia, a disease that causes very high levels of cholesterol and raises your ...
Abstract and Introduction Abstract. Familial Hypercholesterolemia (FH) is a common cause of premature cardiovascular disease and is often undiagnosed in young people.