Paediatric type III dyslipidaemia: a case of vanishing hyperlipidaemia

Gautamn Sarwal, Ahmad AlSarraf, Jiri Frohlich

Research output: Contribution to journalArticle

1 Citation (Scopus)

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.

Original languageEnglish
JournalBMJ case reports
Volume2012
DOIs
Publication statusPublished - 1 Jan 2012

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