Translocation t(1;22) in congenital acute megakaryocytic leukemia

Cancer Genet Cytogenet. 1988 Sep;34(2):277-80. doi: 10.1016/0165-4608(88)90273-7.

Abstract

Acquired chromosomal abnormalities have been reported in 80 patients with congenital acute leukemia, the commonest being t(4;11). We report here a case of acute megakaryocytic leukemia with a rare translocation of t(1;22)(p13.3;q13.3). The course of the disease was short, with the patient surviving less than a year after the initial diagnosis.

Publication types

  • Case Reports
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Chromosomes, Human, Pair 1*
  • Chromosomes, Human, Pair 22*
  • Genetic Markers
  • Humans
  • Infant, Newborn
  • Karyotyping
  • Leukemia, Megakaryoblastic, Acute / congenital*
  • Leukemia, Megakaryoblastic, Acute / genetics
  • Male
  • Translocation, Genetic*

Substances

  • Genetic Markers