Genetic characterization of two 46,XX males without gonadal ambiguities

J Assist Reprod Genet. 2008 Nov-Dec;25(11-12):547-52. doi: 10.1007/s10815-008-9265-7. Epub 2008 Oct 30.

Abstract

Purpose: To evaluate hypotheses which explain phenotypic variability in sex determining region Y positive 46,XX males. We investigate two 46,XX males without gonadal ambiguities.

Methods: Cytogenetic and molecular analyses were used to identify the presence of Y chromosome material and to map the translocation breakpoint. Finally, the pattern of X chromosome inactivation was studied using the methylation assay at the androgen receptor locus.

Results: The presence of Y chromosome material, including the sex determining region Y gene, was demonstrated in both men. However, the amount of translocated Y chromosome material differed between the patients. Different X chromosome inactivation patterns were found in the patients; random in one patient and non-random in the other.

Conclusions: We found a lack of association between phenotype and X chromosome inactivation pattern. Our cytogenetic and molecular analyses show support for the position effect hypothesis explaining the phenotypic variability in XX males.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromosome Mapping
  • DNA / chemistry
  • DNA / genetics
  • Gonadal Dysgenesis, 46,XX / genetics*
  • Humans
  • In Situ Hybridization, Fluorescence
  • Karyotyping
  • Male
  • Phenotype
  • Sex Chromosome Aberrations
  • Sex-Determining Region Y Protein / genetics
  • X Chromosome Inactivation
  • Young Adult

Substances

  • Sex-Determining Region Y Protein
  • DNA