A familial reciprocal translocation t(1;15) in three generations identified in a regular trisomy 21 patient

Genet Couns. 2010;21(3):299-306.

Abstract

The concurrence of a reciprocal translocation and an aneuploidy represent a rare coincidence and an interchromosome effect between these two events has been suggested. We report the case of a family with a t(1;15) in three generations which was identified through the evaluation ofa patient with classical trisomy 21 or Down syndrome. The cytogenetic analysis with GTG banding showed that the proband had a regular trisomy 21 and a balanced translocation t(1;15). FISH and microsatellite analysis were carried out in the family in order to discard an interchromosomal effect. The implications for genetic assessment are discussed.

MeSH terms

  • Aneuploidy*
  • Child, Preschool
  • Chromosome Banding
  • Chromosomes, Human, Pair 1 / genetics*
  • Chromosomes, Human, Pair 15 / genetics*
  • Down Syndrome / diagnosis
  • Down Syndrome / genetics*
  • Female
  • Humans
  • In Situ Hybridization, Fluorescence
  • Infant
  • Infant, Newborn
  • Karyotyping
  • Microsatellite Repeats / genetics
  • Pedigree*
  • Phenotype
  • Translocation, Genetic / genetics*