Paediatric type III dyslipidaemia: a case of vanishing hyperlipidaemia

BMJ Case Rep. 2012 Nov 1:2012:bcr2012007579. doi: 10.1136/bcr-2012-007579.

Abstract

An 11-year-old girl presented with palmar and tuberoeruptive xanthomas, and elevated triglycerides and total cholesterol levels. She had an apolipoprotein E2/E2 genotype. A diagnosis of type III dyslipidaemia was made and the patient started on niacin, fenofibrate and salmon oil. At age 18, her lipid levels were well controlled with fenofibrate once weekly. At age 21, the fenofibrate was discontinued and her lipid profile has been normal for the last 4 years. This case history may be consistent with a transient dyslipidaemia.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Adult
  • Apolipoprotein E2 / genetics
  • Apolipoproteins E / genetics*
  • Child
  • Dyslipidemias / drug therapy
  • Dyslipidemias / genetics*
  • Female
  • Follow-Up Studies
  • Genotype*
  • Humans
  • Hyperlipidemias / drug therapy
  • Hyperlipidemias / genetics*
  • Hyperlipoproteinemia Type III* / drug therapy
  • Hypolipidemic Agents / therapeutic use*
  • Young Adult

Substances

  • Apolipoprotein E2
  • Apolipoproteins E
  • Hypolipidemic Agents