Association of X Chromosome Aberrations with Male Infertility
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20 lis 2021
O artykule
Data publikacji: 20 lis 2021
Zakres stron: 69 - 72
Otrzymano: 11 sie 2020
Przyjęty: 22 wrz 2020
DOI: https://doi.org/10.2478/amb-2021-0051
Słowa kluczowe
© 2021 S. Xharra et al., published by Sciendo
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
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.