Familial Homozygous Hypercholesterolemia is a genetic disorder that leads to extremely high levels of low-density lipoprotein (LDL) cholesterol. This condition significantly increases the risk of premature cardiovascular disease, including heart attacks and strokes.
High Cholesterol, Familial Homozygous FAQ
What is Familial Homozygous Hypercholesterolemia?
Familial Homozygous Hypercholesterolemia is a genetic condition that causes extremely high cholesterol levels, leading to an increased risk of cardiovascular disease.
What are the treatment options for Familial Homozygous Hypercholesterolemia?
Treatment options include medications like mipomersen, lomitapide, and evolocumab, along with lifestyle modifications and dietary changes.
How is Familial Homozygous Hypercholesterolemia diagnosed?
Diagnosis is typically made through genetic testing and lipid profile blood tests to measure cholesterol levels.
What are the risks associated with Familial Homozygous Hypercholesterolemia?
The condition significantly increases the risk of premature cardiovascular diseases such as heart attacks and strokes.
Can lifestyle changes help manage Familial Homozygous Hypercholesterolemia?
Yes, lifestyle changes such as a healthy diet, regular exercise, and avoiding smoking can contribute to managing the condition in conjunction with medications.
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