Association of X Chromosome Aberrations with Male Infertility

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 ch...

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Autores principales:	Xharra S., Behluli E., Moder A., Nefic H., Hadziselimovic R., Temaj G.
Formato:	article
Lenguaje:	EN
Publicado:	Sciendo 2021
Materias:	klinefelter syndrome azoospermia chromosome aberration androgen receptors y chromosome x chromosome Medicine R
Acceso en línea:	https://doaj.org/article/164e01ed5c1c4489bcea8068ba2b2643
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id	oai:doaj.org-article:164e01ed5c1c4489bcea8068ba2b2643
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spelling	oai:doaj.org-article:164e01ed5c1c4489bcea8068ba2b26432021-12-05T14:11:06ZAssociation of X Chromosome Aberrations with Male Infertility2719-538410.2478/amb-2021-0051https://doaj.org/article/164e01ed5c1c4489bcea8068ba2b26432021-11-01T00:00:00Zhttps://doi.org/10.2478/amb-2021-0051https://doaj.org/toc/2719-5384Male 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.Xharra S.Behluli E.Moder A.Nefic H.Hadziselimovic R.Temaj G.Sciendoarticleklinefelter syndromeazoospermiachromosome aberrationandrogen receptorsy chromosomex chromosomeMedicineRENActa Medica Bulgarica, Vol 48, Iss 4, Pp 69-72 (2021)
institution	DOAJ
collection	DOAJ
language	EN
topic	klinefelter syndrome azoospermia chromosome aberration androgen receptors y chromosome x chromosome Medicine R
spellingShingle	klinefelter syndrome azoospermia chromosome aberration androgen receptors y chromosome x chromosome Medicine R Xharra S. Behluli E. Moder A. Nefic H. Hadziselimovic R. Temaj G. Association of X Chromosome Aberrations with Male Infertility
description	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.
format	article
author	Xharra S. Behluli E. Moder A. Nefic H. Hadziselimovic R. Temaj G.
author_facet	Xharra S. Behluli E. Moder A. Nefic H. Hadziselimovic R. Temaj G.
author_sort	Xharra S.
title	Association of X Chromosome Aberrations with Male Infertility
title_short	Association of X Chromosome Aberrations with Male Infertility
title_full	Association of X Chromosome Aberrations with Male Infertility
title_fullStr	Association of X Chromosome Aberrations with Male Infertility
title_full_unstemmed	Association of X Chromosome Aberrations with Male Infertility
title_sort	association of x chromosome aberrations with male infertility
publisher	Sciendo
publishDate	2021
url	https://doaj.org/article/164e01ed5c1c4489bcea8068ba2b2643
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_version_	1718371403520016384

Association of X Chromosome Aberrations with Male Infertility

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