Long-term treatment with recombinant insulin-like growth factor 1 (IGF-1) in a child with IGF-1 gene mutation

Eur J Pediatr. 2010 Feb;169(2):245-7. doi: 10.1007/s00431-009-1004-2. Epub 2009 Jun 11.

Abstract

We assessed the efficacy and safety of recombinant human insulin-like growth factor 1 (IGF-1) therapy over a period of 7.5 years in a child with severe IGF-1 deficiency. Recombinant human IGF-1 was administered subcutaneously in doses between 40 and 80 microg/kg once daily. Height velocity increased from 2 cm/year on average at baseline to 7.9 cm/year during the first year of treatment. In the following years, growth velocity was less but satisfactory during treatment, but decreased when therapy was stopped.

Publication types

  • Case Reports

MeSH terms

  • Child
  • DNA / genetics*
  • DNA Mutational Analysis
  • Follow-Up Studies
  • Humans
  • Injections, Subcutaneous
  • Insulin-Like Growth Factor I / administration & dosage*
  • Insulin-Like Growth Factor I / deficiency
  • Insulin-Like Growth Factor I / genetics*
  • Laron Syndrome / blood
  • Laron Syndrome / drug therapy*
  • Laron Syndrome / genetics
  • Male
  • Mutation*
  • Recombinant Proteins / administration & dosage*
  • Time Factors

Substances

  • Recombinant Proteins
  • Insulin-Like Growth Factor I
  • DNA