Familial translocation 2;17 with partial trisomy 2q32 leads to 2qter

Ann Genet. 1980;23(4):249-50.

Abstract

A case of 2q trisomy in a malformed female infant resulting from unbalanced segregation of maternal origin is reported. The mother and one of the proposita's sibs where found to be carriers of balanced translocation 2;17. Two other members in the kindred had died with multiple malformations. The patient's karyotype was 46,XX,-17, + der (17)t(2;17)(q32;q25)mat.

Publication types

  • Case Reports

MeSH terms

  • Chromosome Aberrations / genetics*
  • Chromosome Disorders
  • Chromosomes, Human, 1-3*
  • Female
  • Humans
  • Infant, Newborn
  • Translocation, Genetic*
  • Trisomy*