• Deficit in Social Cognitive Abilities Among PWS Children Linked to Genetic Subtype, Study Says
  • Birth Weight and Length May Help Identify Newborns with Prader-Willi Syndrome
  • ‘Disorder’ Film Festival Offers Look at Siblings Touched by Rare Diseases
  • Both Surgery, Cast Correction Effective in Treating Early-onset Scoliosis in PWS Children, Study Reports
  • At NY Genome Center, Legal Expert Presents Ethical Dilemmas in Gene Editing
  • Saniona Sets Goals for its Clinical Program of Tesomet for PWS
  • FPWR Research Symposium and Family Conference Set for Oct. 3-5 in New Orleans
  • Patients Treated With Growth Hormone Score Higher on Vocabulary IQ Tests, Study Shows
  • Nebraska’s Neena Nizar Seeks Cure for Jansen’s, One of World’s Rarest Diseases
  • Factors Such as Older Age, Obesity, and Heart Disease Raise Risk of Blood Clots in PWS Patients, U.S. Survey Says
  • Inhibiting Epigenetic Enzyme May Help Reactivate Key PWS Genes, Study Suggests
  • Millendo Therapeutics Announces Phase 2b/3 Trial Assessing Promising PWS Therapy, Livoletide