Transient hypertriglyceridemia of infancy

Acta Paediatr. 1996 Dec;85(12):1508-10. doi: 10.1111/j.1651-2227.1996.tb13964.x.

Abstract

A premature boy who had suffered from IRDS, bronchopulmonary dysplasia and retinopathy of prematurity developed massive hypertriglyceridemia (48.1 mmol/L) together with moderate hypercholesterolemia (12.6 mmol/L) at 5 months of age. Lipoprotein electrophoresis revealed a marked elevation of the level of the very low density lipoprotein fraction. There was a moderate decrease in the activity of a lipolytic enzyme, lipoprotein lipase (LPL). The child had neither liver or renal disorder nor any inflammatory disease. The hyperlipidemia disappeared spontaneously at the age of 3 years. The cause of the decreased LPL activity could not be established. A partial genetic deficiency in lipoprotein lipase appears the most likely explanation, since no signs of secondary lowering of LPL activity could be found.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Child, Preschool
  • Humans
  • Hypercholesterolemia / complications
  • Hypertriglyceridemia* / enzymology
  • Infant
  • Infant, Newborn
  • Infant, Premature
  • Lipoprotein Lipase / blood
  • Lipoproteins, VLDL / blood
  • Male
  • Remission, Spontaneous

Substances

  • Lipoproteins, VLDL
  • Lipoprotein Lipase