Microdeletions in the Y chromosome of patients with idiopathic azoospermia

Asian J Androl. 2002 Jun;4(2):111-5.

Abstract

Aim: To evaluate the occurrence and prevalence of microdeletions in the gamma chromosome of patients with azoospermia.

Methods: DNA from 29 men with idiopathic azoospermia was screened by polymerase chain reaction (PCR) analysis with a set of gamma chromosome specific sequence-tagged sites (STSs) to determine microdeletions in the gamma chromosome.

Results: Deletions in the DAZ (deleted in azoospermia) loci sgamma254 and sgamma255 were found in three patients with idiopathic azoospermia, resulting in an estimated frequency of deletions of 10.7% in idiopathic azoospermia men.

Conclusion: We conclude that PCR analysis is useful for the diagnosis of microdeletions in the Y chromosome, which is important when deciding the suitability of a patient for assisted reproductive technology such as testicular sperm extracion-intracytoplasmic sperm injection (TESE-ICSI).

MeSH terms

  • Adult
  • Base Sequence
  • Chromosomes, Human, Y*
  • DNA Primers
  • Euchromatin / genetics
  • Follicle Stimulating Hormone / blood
  • Heterochromatin / genetics
  • Humans
  • Luteinizing Hormone / blood
  • Male
  • Oligospermia / blood
  • Oligospermia / etiology
  • Oligospermia / genetics*
  • Polymerase Chain Reaction
  • Prolactin / blood
  • Sequence Deletion / genetics*
  • Sequence Tagged Sites
  • Testosterone / blood

Substances

  • DNA Primers
  • Euchromatin
  • Heterochromatin
  • Testosterone
  • Prolactin
  • Luteinizing Hormone
  • Follicle Stimulating Hormone