Molecular and cytogenetic characterization of a structural rearrangement of the Y chromosome in an azoospermic man

Fertil Steril. 2004 May;81(5):1388-90. doi: 10.1016/j.fertnstert.2003.09.069.

Abstract

Objective: To better define an abnormal karyotype found in a male with primary infertility.

Design: Case report.

Setting: Molecular and cytogenetics unit in a university-affiliated hospital.

Patient(s): A 41-year-old, azoospermic, but otherwise healthy male.

Intervention(s): Lymphocytic karyotype and genetic counseling.

Main outcome measure(s): Metaphases were studied by standard G- and Q-banding, followed by fluorescence in situ hybridization (FISH) and polymerase chain reaction to analyze specific Y chromosome regions.

Result(s): Chromosomal analysis and FISH allowed us to define the propositus's karyotype as 45,X/46,X,idic(Yp)/46,XY (71%, 26%, and 3% of analyzed metaphases, respectively). Molecular analysis of azoospermic factor (AZF) regions showed deletion of AZFb and AZFc.

Conclusion(s): A 45,X/46,X,idic(Yp) mosaicism is associated with a very broad spectrum of phenotypes, including patients with Ullrich-Turner syndrome, patients with various degrees of genital ambiguity, or normal males. In the presence of a normal masculinization in otherwise healthy males azoospermia is a distinct feature that can be explained by partial deletion of AZF regions.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Chromosome Deletion
  • Chromosomes, Human, Y*
  • Humans
  • In Situ Hybridization, Fluorescence
  • Karyotyping
  • Male
  • Oligospermia / genetics*
  • Sex Chromosome Aberrations*