Congenital acute lymphoblastic leukemia with chromosomal abnormalities including a translocation (1;4;22)

Cancer Genet Cytogenet. 1983 Sep;10(1):37-42. doi: 10.1016/0165-4608(83)90103-6.

Abstract

Cytogenetic studies in a patient with inborn ALL demonstrated identical and complex abnormalities in all the cells, indicating a monoclonal origin. These abnormalities included, among others, a translocation (1;4;22).

Publication types

  • Case Reports

MeSH terms

  • Chromosome Aberrations*
  • Chromosome Disorders*
  • Chromosomes, Human, 1-3*
  • Chromosomes, Human, 21-22 and Y*
  • Chromosomes, Human, 4-5*
  • Humans
  • Infant, Newborn
  • Infant, Newborn, Diseases / genetics*
  • Karyotyping
  • Leukemia / congenital
  • Leukemia / genetics
  • Leukemia, Lymphoid / congenital
  • Leukemia, Lymphoid / genetics*
  • Male
  • Translocation, Genetic*