Variants of the GNAI1 gene manifest as Prader-Willi-like syndrome: Case report with literature review

Clin Dysmorphol. 2024 Apr 1;33(2):69-74. doi: 10.1097/MCD.0000000000000491. Epub 2024 Feb 28.
No abstract available

Publication types

  • Review
  • Case Reports

MeSH terms

  • Chromosome Disorders*
  • Developmental Disabilities*
  • Facies*
  • Humans
  • Hypopituitarism*
  • Imprinting Disorders*
  • Syndrome*

Substances

  • Schaaf-Yang syndrome