[Comments on the article <<Neonatal cholestasis revealing an intermediate phenotype of Gaucher disease, type 2>>]

Arch Pediatr. 2009 Aug;16(8):1190-1. doi: 10.1016/j.arcped.2009.04.012. Epub 2009 Jun 10.
[Article in French]
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Cholestasis / diagnosis
  • Cholestasis / drug therapy
  • Cholestasis / genetics*
  • Fatal Outcome
  • Gaucher Disease / diagnosis
  • Gaucher Disease / drug therapy
  • Gaucher Disease / genetics*
  • Glucosylceramidase / administration & dosage
  • Humans
  • Infant, Newborn
  • Infusions, Intravenous
  • Jaundice, Neonatal / diagnosis
  • Jaundice, Neonatal / drug therapy
  • Jaundice, Neonatal / genetics*
  • Male
  • Phenotype*
  • Recombinant Proteins / administration & dosage

Substances

  • Recombinant Proteins
  • Glucosylceramidase
  • imiglucerase