The Arduous Path to Drug Approval for the Management of Prader-Willi Syndrome: A Historical Perspective and Call to Action

Int J Mol Sci. 2023 Jul 18;24(14):11574. doi: 10.3390/ijms241411574.

Abstract

Prader-Willi syndrome (PWS) is a neuroendocrine genetic disorder resulting from the loss of paternally expressed imprinted genes in chromosome 15q11-q13 [...].

Publication types

  • Editorial

MeSH terms

  • Chromosomes
  • Chromosomes, Human, Pair 15 / genetics
  • Drug Approval
  • Genomic Imprinting
  • Humans
  • Prader-Willi Syndrome* / drug therapy
  • Prader-Willi Syndrome* / genetics