Marker chromosome 1q+ in acute lymphocytic leukemia

Cancer Genet Cytogenet. 1987 Feb;24(2):251-5. doi: 10.1016/0165-4608(87)90106-3.

Abstract

This paper presents the results of a cytogenetic analysis on a patient with acute lymphocytic leukemia (ALL) type L2 according to the FAB classification. Of the metaphases examined, 69.3% belong to the aberrant clone of pseudodiploid karyotype. Marker chromosome 14q+ has been identified in all the cells of the clone. Duplication was found in 30% of the metaphases, and in 15% triplication of the proximal segment of the long arm of chromosome #1 (q11-q21). In one metaphase the long arm of chromosome #1 is made up of segment q11-q21 four times repeated. Aberrations of chromosome #1 support the idea that heterochromatic region may be related to the higher degree of the cell malignity.

Publication types

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

MeSH terms

  • Adolescent
  • Chromosome Aberrations*
  • Chromosome Banding
  • Chromosomes, Human, Pair 1*
  • Genetic Markers*
  • Humans
  • Karyotyping
  • Leukemia, Lymphoid / genetics*
  • Male
  • Multigene Family

Substances

  • Genetic Markers