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Familial Hypercholesterolemia

Familial Hypercholesterolemia (FH) is a genetic condition that results in very high levels of cholesterol in the blood, significantly increasing the risk of heart disease and stroke. It occurs when a person inherits a faulty gene from one or both parents that affects the body's ability to remove low-density lipoprotein (LDL) cholesterol, often referred to as "bad cholesterol." Individuals with FH may develop heart problems at an early age, so early diagnosis and management, often involving lifestyle changes and medications, are crucial for reducing health risks. Regular check-ups and cholesterol monitoring are essential for those affected.

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    Familial hypercholesterolemia is a genetic condition that causes very high levels of cholesterol in the blood. This happens because the body is unable to remove low-density lipoprotein (LDL) cholesterol effectively. People with this condition often have a family history of high cholesterol, heart disease, or early heart attacks. If untreated, it can lead to serious cardiovascular issues. Management typically involves lifestyle changes and medications to lower cholesterol levels, and early detection is crucial to prevent complications. Regular check-ups and family screening are important for those with a family history of the disorder.