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SNORD116 and growth hormone therapy impact IGFBP7 in Prader-Willi syndrome.

Sanaa EddiryGwenaelle DieneCatherine MolinasJuliette SallesFrançoise Conte AuriolIsabelle GenneroEric BiethBoris V SkryabinTimofey S RozhdestvenskyLisa C BurnettRudolph L LeibelMaithé TauberJean Pierre Salles
Published in: Genetics in medicine : official journal of the American College of Medical Genetics (2021)
SNORD116 deletion affects IGFBP7 levels, while IGFBP7 decreases under GHT in PWS patients. Modulation of the IGFBP7 level, which interacts with IGF1, has implications in the pathophysiology and management of PWS under GHT.
Keyphrases
  • growth hormone
  • end stage renal disease
  • ejection fraction
  • newly diagnosed
  • peritoneal dialysis
  • stem cells
  • binding protein
  • case report
  • cell proliferation
  • bone marrow
  • patient reported outcomes