An inherited disorder that increases a person’s risk for high cholesterol
People with familial cholesterolemia have a genetic mutation that changes how the body processes cholesterol. This can increase your risk of atherosclerosis, or clogged arteries, and heart disease at a young age.
The gene mutation is passed on from parent to child. If one parent has familial hypercholesterolemia, each child has a 50 percent risk of having the disorder. If both parents have the genetic mutation, their child may have a more severe form of the disorder.
Tests
Diagnosing a potential heart or vascular condition is the first step to developing a treatment plan. Our specialists may recommend one or more diagnostic and imaging procedures.
Treatments
While lifestyle modifications, such as eating a healthy diet and exercising regularly, are the first line of defense, most people with familial hypercholesterolemia also will need to take a cholesterol-lowering medication.
Our providers
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Cardiology
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Dweep Barbhaya, MD
Cardiology & Hospital Medicine
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Barbara Louise Bean, MD
Cardiology
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Jee Young Choi, ACNP-BC
Cardiology
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Karim Hemady, PA-C
Cardiology
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Kristina Marie Hidalgo, ACNP-BC
Cardiology
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Cathryn Hodukavich, ACNP-BC
Cardiology
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Brooke Elizabeth Huggins, PA-C
Cardiology
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Wahu Kinyanjui Johnson, AGACNP-BC
Cardiology
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Tiffany K. McKenzie, AGACNP-BC
Cardiology
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Robin Nebbia, NP
Cardiology
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Virginia E. Seay, CRNP
Cardiology
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Narayana Sarma V Singam, MD
Cardiology & Critical Care Medicine
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Laura Keiler Topper, CRNP,ANP,BC
Cardiology
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Federico Viganego, MD
Cardiology
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Newton Edison Andrews, MD
Cardiology
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Alfred Burris, MD
Cardiology
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