der(1;15)(q10;10): a nonrandom chromosomal abnormality of myeloid neoplasia

Cancer Genet Cytogenet. 1995 Sep;83(2):144-7. doi: 10.1016/0165-4608(95)00041-m.

Abstract

The occurrence of an unusual karyotypic abnormality der(1;15)(q10;q10) is reported in three patients, one with acute megakaryoblastic leukemia and two with myelodysplastic syndrome. A literature review shows that this cytogenetic abnormality is a rare but nonrandom change in myeloid neoplasia/neoplasia.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Aged
  • Child, Preschool
  • Chromosomes, Human, Pair 1*
  • Chromosomes, Human, Pair 15*
  • Female
  • Humans
  • Karyotyping
  • Leukemia, Megakaryoblastic, Acute / genetics*
  • Male
  • Middle Aged
  • Myelodysplastic Syndromes / genetics*
  • Translocation, Genetic*