Myeloproliferative disorder in a patient with RIT1-associated Noonan syndrome: Case report and literature review

Pediatr Blood Cancer. 2024 Feb;71(2):e30780. doi: 10.1002/pbc.30780. Epub 2023 Nov 27.
No abstract available

Publication types

  • Review
  • Case Reports
  • Letter

MeSH terms

  • Humans
  • Mutation
  • Myeloproliferative Disorders* / complications
  • Myeloproliferative Disorders* / genetics
  • Noonan Syndrome* / complications
  • Noonan Syndrome* / genetics
  • ras Proteins / genetics

Substances

  • RIT1 protein, human
  • ras Proteins