A case of Behcet's disease associated with myelodysplastic syndrome involving trisomy 8 and a gain-of-function mutation in SHP-2

Rheumatology (Oxford). 2011 Jul;50(7):1342-4. doi: 10.1093/rheumatology/ker137. Epub 2011 Apr 10.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Behcet Syndrome / complications
  • Behcet Syndrome / genetics
  • Behcet Syndrome / immunology*
  • Child, Preschool
  • Chromosomes, Human, Pair 8 / genetics
  • Female
  • Follow-Up Studies
  • Humans
  • Immunity, Innate / genetics
  • Mutation*
  • Myelodysplastic Syndromes / complications
  • Myelodysplastic Syndromes / genetics
  • Myelodysplastic Syndromes / immunology*
  • Protein Tyrosine Phosphatase, Non-Receptor Type 11 / genetics*
  • Rare Diseases
  • Risk Assessment
  • Trisomy / diagnosis*
  • Trisomy / genetics

Substances

  • Protein Tyrosine Phosphatase, Non-Receptor Type 11

Supplementary concepts

  • Chromosome 8, trisomy