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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Ebony Rebecca Alston, MD
Cardiology
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Rahul Anand, MD
Cardiology
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Rachel Barish, CRNP
Cardiology
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Patrick Thomas Bering, MD
Cardiac Imaging & Cardiology
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Shen Cao, PA-C
Cardiology
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Louis K Essandoh, MD
Cardiology
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Preetham N. Kumar, MD
Cardiac Imaging & Cardiology
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Bryan LeBude, MD
Cardiology
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William Clarence Maxted, MD
Cardiology
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Etonde Mafany Musonge-Tarkang, MD
Cardiology
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Robin Nebbia, NP
Cardiology
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Shreya Rao, PA-C
Cardiology
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Monil Rajeshbhai Shah, MD
Cardiology
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Athanasios Thomaides, MD
Cardiology & Electrophysiology
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Alfred Burris, MD
Cardiology
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Gopalakrishnan Srinivasan, MD
Cardiology
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