Primary male infertility in Izmir/Turkey: a cytogenetic and molecular study of 187 infertile Turkish patients

  • Haluk Akin
  • Huseyin Onay
  • Emre Turker
  • Ferda Ozkinay
Genetics

Abstract

Purpose

To detect somatic cytogenetic abnormalities and AZF microdeletions in a sample of 187 Turkish infertile men to determine the frequencies and the characteristics of our primary male infertility data in order to perform appropriate genetic counseling.

Methods

This study included 187 infertile men. Chromosomal studies and screening of AZF deletions was performed by multiplex polymerase chain reaction (PCR) analysis using the Y Chromosome Deletion Detection System.

Results

Cytogenetic study revealed chromosomal abnormality in 9 subjects (4.8%). In remaining 178 subjects, 7 subjects (3.93%) were detected to have Y chromosome microdeletions. The AZFc region was the most frequently involved region in microdeletion process in affected subjects. All subjects having microdeletion were azoospermic

Conclusions

Cytogenetic and molecular study should be performed to obtain reliable genetic information for the genetic counseling of primary infertile man. Y chromosome microdeletion diagnosis is useful in decision making for assisted reproductive technics.

Keywords

Primary male infertiliy Genetic factors Y chromosome Microdeletions 

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Copyright information

© Springer Science+Business Media, LLC 2011

Authors and Affiliations

  • Haluk Akin
    • 1
  • Huseyin Onay
    • 1
  • Emre Turker
    • 1
  • Ferda Ozkinay
    • 1
  1. 1.Department of Medical Genetics School of MedicineEge UniversityIzmırTurkey

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