Identification of Y-chromosomal DNA in a Turner syndrome mosaic by polymerase chain reaction

Ann Genet. 1991;34(3-4):252-5.

Abstract

A 15.5-year-old female was referred for primary amenorrhea and slow development of secondary sex characteristics. The karyotype revealed 45,X/46,X,+mar (75%/25%). The small marker chromosome was C-band and Q-band negative. It appeared to be primarily centromeric with some light G-band staining material on either side. Females with Y-chromosomal material are at an increased risk for gonadal neoplasia and this patient was studied further to investigate the possibility that the marker was a deleted Y chromosome. Polymerase chain reaction (PCR) analysis of this patient's DNA revealed the presence of Y-chromosomal material presumably derived from the marker chromosome. These results indicate that the PCR technique, in conjunction with cytogenetic analysis, can identify possible Y-chromosomal material. This testing provides critical information necessary for correct medical followup of Turner syndrome mosaic patients.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • DNA / analysis*
  • Female
  • Genetic Markers / genetics
  • Humans
  • Karyotyping
  • Mosaicism / genetics*
  • Polymerase Chain Reaction
  • Sex Chromosome Aberrations / genetics
  • Turner Syndrome / genetics*
  • Y Chromosome*

Substances

  • Genetic Markers
  • DNA