Acta Medica Bulgarica (Nov 2021)

Association of X Chromosome Aberrations with Male Infertility

  • Xharra S.,
  • Behluli E.,
  • Moder A.,
  • Nefic H.,
  • Hadziselimovic R.,
  • Temaj G.

DOI
https://doi.org/10.2478/amb-2021-0051
Journal volume & issue
Vol. 48, no. 4
pp. 69 – 72

Abstract

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Male infertility is caused by spermatogenetic failure, clinically noted as oligoor azoospermia. Approximately 20% of infertile patients carry a genetic defect. The most frequent genetic defect leading to azoospermia (or severe oligozoospermia) is Klinefelter syndrome (47, XXY), which is numerical chromosomal abnormality and Y- structural chromosome aberration. The human X chromosome is the most stable of all human chromosomes. The X chromosome is loaded with regions of acquired, rapidly evolving genes. The X chromosome may actually play an essential role in male infertility and sperm production. Here we will describe X chromosome aberrations, which are associated with male infertility.

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