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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Ann Mary Graham Acosta, AGACNP-BC,BC,AGCNS,DNP
Cardiology
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Najdat Bazarbashi, MD
Cardiology
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Lindsay Nicole Bussey, FNP-BC,CRNP
Cardiology
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Shen Cao, PA-C
Cardiology
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Ruchi Pratik Desai, PA-C
Cardiology
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Sherron Hester-Bello, FNPBC
Cardiology
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Likhitesh Gunjur Jaikumar, MD
Cardiology
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Kriti Kalra, MD
Cardiology
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Brittany A. Muchla, CRNP,C,FNP
Cardiology
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Ricardo Andres Nieves, MD
Cardiology
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Shreya Rao, PA-C
Cardiology
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Monil R. Shah, MD
Cardiology
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Federico Viganego, MD
Cardiology
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Sara E. Wanner, CRNP,ACNP,BC
Cardiology
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Joseph Adolph Quash, MD
Cardiology
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Nichole Lasha Williams, FNP-C
Cardiology
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