Familial lipid disorders


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Familial lipid disorders


A familial lipid disorder is an inherited condition that causes very high levels of cholesterol and, in some cases, triglycerides. Familial lipid disorders often result in the premature onset of coronary artery disease (CAD). Because familial lipid disorders are rare, your doctor may only suspect one if you have:

Because familial lipid disorders are so rare, your primary care doctor may not have a great deal of experience in dealing with them. In this case, you may need to see a doctor who specializes in these conditions. Because familial lipid disorders often result in early CAD, a number of cardiologists specialize in lipid disorders as well as heart problems.

Types of familial lipid disorders

Disorder

Cholesterol level

Distinguishing characteristics

Familial combined hyperlipidemia (FCHL)
Familial defective apolipoprotein B-100  
Familial dysbetalipoproteinemia (type 3 hyperlipoproteinemia)
  • Total cholesterol of 300–600 mg/dL
  • Triglyceride of 400–800 mg/dL
Familial hypertriglyceridemia
  • Very high triglycerides
  • Risk for even higher triglycerides from secondary causes
Heterozygous familial hypercholesterolemia
  • Total cholesterol of 325–450 mg/dL
  • CAD before age 50
  • Small, pale ring around the iris of the eye
  • Xanthomas on tendons in young adults
Homozygous familial hypercholesterolemia
  • Total cholesterol of 500–1,000 mg/dL
  • CAD before age 20
  • Xanthomas on tendons within the first few months of life

Credits


Author Robin Parks, MS
Editor Kathleen M. Ariss, MS
Associate Editor Pat Truman, MATC
Primary Medical Reviewer E. Gregory Thompson, MD - Internal Medicine
Specialist Medical Reviewer Robert A. Kloner, MD, PhD - Cardiology
Last Updated July 11, 2008

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Last updated: July 11, 2008
Author: Robin Parks, MS
Reviewed By: E. Gregory Thompson, MD - Internal Medicine, Robert A. Kloner, MD, PhD - Cardiology
Editors: Kathleen M. Ariss, MS, Pat Truman, MATC

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