Cytogenetics of infantile leukemias and its correlations with bio-clinical features. The "G. Gaslini" Children's Hospital experience over a 9-year period

Haematologica. 1991 Mar-Apr;76(2):109-12.

Abstract

Background and methods: Infantile leukemia is a rare disorder, and few cytogenetic studies have been performed on this condition.

Results and conclusions: The authors present the cytogenetic analyses performed on 14 cases of infantile leukemia. The most frequent chromosomal changes are rearrangements involving 11q (4 cases) and gains of one or more chromosomes 21. Patients with chromosomal rearrangements show a worse prognosis than those with only hyperdiploidy or a normal karyotype, although the difference was not statistically significant due to the small size and short median follow-up.

MeSH terms

  • Chromosome Aberrations*
  • Chromosomes, Human, Pair 11 / ultrastructure
  • Chromosomes, Human, Pair 21
  • Female
  • Follow-Up Studies
  • Hospitals, Pediatric
  • Humans
  • Infant
  • Italy
  • Leukemia / genetics*
  • Leukemia / mortality
  • Male
  • Ploidies
  • Prognosis
  • Survival Rate