Transient myeloproliferative disorder in an infant with PTPN11 mutation

Br J Haematol. 2017 Apr;177(1):11. doi: 10.1111/bjh.14517. Epub 2017 Jan 20.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Blood Cells / pathology
  • Bone Marrow / pathology
  • DNA Mutational Analysis
  • Down Syndrome / diagnosis*
  • Down Syndrome / genetics*
  • Female
  • Humans
  • Infant
  • Infant, Newborn
  • Leukemoid Reaction / diagnosis*
  • Leukemoid Reaction / genetics*
  • Mutation*
  • Protein Tyrosine Phosphatase, Non-Receptor Type 11 / genetics*

Substances

  • PTPN11 protein, human
  • Protein Tyrosine Phosphatase, Non-Receptor Type 11

Supplementary concepts

  • Myeloproliferative Syndrome, Transient