Genetic Familial Hypercholesterolaemia (FH) Blood Test detects genetic cholesterol issues.
The Genetic Familial Hypercholesterolaemia (FH) Blood Test is a crucial diagnostic tool for identifying individuals with FH, a genetic disorder that results in high cholesterol levels. This test is essential in preventing premature heart disease and managing cholesterol levels effectively.
The test primarily looks for mutations in three genes: LDLR, PCSK9, and APOB. These mutations are commonly associated with FH. However, the specific set of biomarkers may vary slightly depending on the provider.
The results of the Hypercholesterolaemia Blood Test can guide treatment plans and lifestyle changes. Early detection of FH can significantly reduce the risk of premature heart disease and other complications.
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The cost of Genetic Familial Hypercholesterolaemia (FH) may be covered by private health insurance plans, depending on the specifics of the policy. Check with your insurance provider to understand what is covered.
Familial Hypercholesterolaemia (FH) is a genetic disorder that results in high cholesterol levels, increasing the risk of premature heart disease. It is diagnosed through a Genetic FH Blood Test that looks for mutations in specific genes.
The Genetic FH Blood Test looks for mutations in three genes: LDLR, PCSK9, and APOB. These mutations are commonly associated with Familial Hypercholesterolaemia.
The results of the Genetic FH Blood Test can guide treatment plans and lifestyle changes. Early detection of FH can significantly reduce the risk of premature heart disease and other complications.
The cost of the Genetic FH Blood Test in the UK typically ranges from £150 to £350, inclusive of appointment fees.
No, a doctor's referral is not necessary for this test. A self-referral allows you to book a private appointment directly with the provider.
Individuals with a family history of high cholesterol or premature heart disease may consider this test. Symptoms of FH include high LDL cholesterol levels, fatty skin deposits, and cholesterol deposits around the cornea.
The appointment typically lasts about an hour. A small blood sample will be taken for genetic screening analysis. There is no need to fast for this test.
The analysis involves sequencing the genes associated with FH. If a mutation is found, it indicates a positive diagnosis for FH. The results are usually available within 2 to 4 weeks.
For more information about FH, visit Heart UK or British Heart Foundation.
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