Familial Hypercholesterolemia

Familial hypercholesterolemia (FH) is a genetic disorder that leads to abnormally high levels of cholesterol in the blood. It is often underdiagnosed, as most individuals with FH do not have the classic symptoms, but it can lead to serious physical issues such as heart disease and stroke. FH can be managed with lifestyle changes, such as diet and exercise, as well as cholesterol-lowering medications. Early diagnosis and proper management of FH can greatly reduce the risk of long-term health complications.

← Journal of Proteomics and Genomics Research

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Molecular and Metabolic Pathogenesis of Familial Combined Hyperlipidemia and Association with Metabolic Syndrome

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