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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Rebecca Michelle Burton, BS, MHS, PA-C, AAS
Cardiology
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Zelda J Diamond, FNP, FNPBC
Cardiology
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Daniel James Dooley, MD
Cardiology
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Laura Jean Hachani, MHS, PA, vCER
Cardiology
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Sherron Hester-Bello, FNPBC, MSN
Cardiology
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Marcus D. Hodge, MPAS, PA
Cardiology
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Mark Robert Hofmeyer, MD
Cardiology & Heart Failure And Transplantation Cardiology
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Jordan Ashley Kane, PA-C, MMPAS
Cardiology
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Kerunne Segametsi Ketlogetswe, MD
Cardiology
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Rahul Malik, MD
Cardiology
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Chinwe Mueller, ACNP-BC, MSN
Cardiology
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Ainsley Anthony O'Garro, PA, PA-C
Cardiology
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Awail Sadiq, MD
Cardiology
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Stuart Floyd Seides, MD
Cardiology
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Jaclyn Sesso, DNP
Cardiology
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Donna S. Westervelt, CRNP
Cardiology
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