Prader-Willi syndrome

Lancet. 2000 Aug 19;356(9230):673-5. doi: 10.1016/s0140-6736(00)02617-9.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Chromosomes, Human, Pair 15 / genetics
  • Female
  • Genomic Imprinting
  • Humans
  • Hyperphagia
  • Hypogonadism
  • Intellectual Disability
  • Muscle Hypotonia
  • Prader-Willi Syndrome / diagnosis*
  • Prader-Willi Syndrome / genetics
  • Prader-Willi Syndrome / therapy