Identification of a whole-arm translocation by in situ hybridization with directly fluorochrome-labeled probes in a myelodysplastic syndrome

Genes Chromosomes Cancer. 1992 Sep;5(2):128-31. doi: 10.1002/gcc.2870050206.

Abstract

A case of myelodysplasia was found to have a complex bone marrow karyotype, involving an apparent whole-arm translocation between 17q and 18q. The application of a simplified fluorescence in situ hybridization technique, using directly fluorochrome-labeled centromere-specific alpha-satellite DNA probes, demonstrated the presence of sequences from both chromosomes 17 and 18 in the centromere of the derivative chromosome. This proves that a true whole-arm translocation had occurred. The case exemplifies how in situ hybridization analysis can be used to resolve interpretation problems in cancer cytogenetics.

Publication types

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

MeSH terms

  • Aged
  • Chromosomes, Human, Pair 17*
  • Chromosomes, Human, Pair 18*
  • DNA Probes / genetics
  • DNA, Satellite / genetics
  • Fluorescence
  • Humans
  • Male
  • Myelodysplastic Syndromes / genetics*
  • Nucleic Acid Hybridization*
  • Translocation, Genetic / genetics*

Substances

  • DNA Probes
  • DNA, Satellite