Dicentric chromosome Y associated with Leydig cell agenesis and sex reversal

Clin Genet. 1995 Jan;47(1):38-41. doi: 10.1111/j.1399-0004.1995.tb03919.x.

Abstract

The nature of a non-mosaic marker Y chromosome observed in a pseudohermaphrodite patient with Leydig cell agenesis was investigated by high-resolution chromosome analysis and molecular probes from the Y chromosome. Cytogenetically, the marker chromosome appeared to be an isodicentric, with breakage in Yq11.21. Double copies of all Yp-specific loci tested, including SRY, were present. The most distal Yq portion detected in patient DNA was DXS278-C, which maps to interval D in the chromosome Yq deletion map. Fragment DXS278-B, which maps to deletion interval E, was absent. The possible relationship between this cytogenetic abnormality and Leydig cell agenesis, a finding never reported in association with Y chromosome rearrangements, is discussed.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Disorders of Sex Development*
  • Genetic Markers
  • Humans
  • Karyotyping
  • Leydig Cells / ultrastructure*
  • Male
  • Sex Chromosome Aberrations*
  • Testis / abnormalities*
  • Y Chromosome*

Substances

  • Genetic Markers