Double 20q- anomaly in myelodysplastic syndrome

Cancer Genet Cytogenet. 1992 Feb;58(2):174-6. doi: 10.1016/0165-4608(92)90107-j.

Abstract

Two patients with myelodysplastic syndrome (MDS) whose bone marrow (BM) cells contained duplicate 20q- chromosomes are reported. No particular differences between the hematologic findings of four patients with single 20q- and the two patients with double 20q- chromosomes were noted. No differences in breakpoints on the 20q- chromosome were noted in these six patients, and the breakpoint was identified as 20q11. The presence of double 20q- chromosomes in MDS patients suggests, however, that the deleted chromosome has oncogenic activity.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Bone Marrow / pathology*
  • Chromosome Aberrations*
  • Chromosome Banding
  • Chromosomes, Human, Pair 20*
  • Female
  • Humans
  • Karyotyping
  • Male
  • Myelodysplastic Syndromes / genetics*
  • Myelodysplastic Syndromes / pathology*