Mosaic ring Y chromosome in two normal healthy men with azoospermia
To better define by molecular and cytogenetic techniques ring Y chromosomes detected in 2 infertile men. Case report. Molecular genetics/cytogenetics unit in a university hospital. Two infertile men with azoospermia, presenting a normal male phenotype with complete masculinization. Karyotype and gen...
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Veröffentlicht in: | Fertility and sterility 2005-12, Vol.84 (6), p.1744.e1-1744.e4 |
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creator | Bertini, Veronica Canale, Domenico Bicocchi, Maria Patrizia Simi, Paolo Valetto, Angelo |
description | To better define by molecular and cytogenetic techniques ring Y chromosomes detected in 2 infertile men.
Case report.
Molecular genetics/cytogenetics unit in a university hospital.
Two infertile men with azoospermia, presenting a normal male phenotype with complete masculinization.
Karyotype and genetic counseling.
Metaphases were studied by standard G- and Q-banding; fluorescent in situ hybridization and PCR were performed to analyze specific Y chromosome regions.
Chromosomal analysis detected a mosaicism with a Y chromosome ring cell line in 92% (patient 1) and 95% (patient 2) of the metaphases, coexisting with a 45,X cell line in the remaining metaphases. In patient 1, PCR analysis showed the presence of AZFa region and a partial deletion of AZFb region; AZFc region was deleted. In patient 2 all three AZF regions were deleted.
A 45,X/46,X,r(Y) mosaicism can be detected not only in patients with Ullrich-Turner syndrome and in patients with various degrees of genital ambiguity but also in men presenting a normal phenotype. Their azoospermia can be explained by partial or total deletion of AZF regions. |
doi_str_mv | 10.1016/j.fertnstert.2005.06.034 |
format | Article |
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Case report.
Molecular genetics/cytogenetics unit in a university hospital.
Two infertile men with azoospermia, presenting a normal male phenotype with complete masculinization.
Karyotype and genetic counseling.
Metaphases were studied by standard G- and Q-banding; fluorescent in situ hybridization and PCR were performed to analyze specific Y chromosome regions.
Chromosomal analysis detected a mosaicism with a Y chromosome ring cell line in 92% (patient 1) and 95% (patient 2) of the metaphases, coexisting with a 45,X cell line in the remaining metaphases. In patient 1, PCR analysis showed the presence of AZFa region and a partial deletion of AZFb region; AZFc region was deleted. In patient 2 all three AZF regions were deleted.
A 45,X/46,X,r(Y) mosaicism can be detected not only in patients with Ullrich-Turner syndrome and in patients with various degrees of genital ambiguity but also in men presenting a normal phenotype. Their azoospermia can be explained by partial or total deletion of AZF regions.</description><identifier>ISSN: 0015-0282</identifier><identifier>EISSN: 1556-5653</identifier><identifier>DOI: 10.1016/j.fertnstert.2005.06.034</identifier><identifier>PMID: 16359976</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; AZF regions ; Azoospermia ; Chromosomes, Human, Y ; FISH ; Humans ; In Situ Hybridization, Fluorescence ; infertile male ; Male ; Mosaicism ; Oligospermia - genetics ; Ring Chromosomes ; ring Y chromosome ; Sex Chromosome Aberrations</subject><ispartof>Fertility and sterility, 2005-12, Vol.84 (6), p.1744.e1-1744.e4</ispartof><rights>2005 American Society for Reproductive Medicine</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3374-f4e099572eff779837714f7e148d024268fe05ccdbf7ad5e70c1bf17acbdf0c23</citedby><cites>FETCH-LOGICAL-c3374-f4e099572eff779837714f7e148d024268fe05ccdbf7ad5e70c1bf17acbdf0c23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0015028205033303$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16359976$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bertini, Veronica</creatorcontrib><creatorcontrib>Canale, Domenico</creatorcontrib><creatorcontrib>Bicocchi, Maria Patrizia</creatorcontrib><creatorcontrib>Simi, Paolo</creatorcontrib><creatorcontrib>Valetto, Angelo</creatorcontrib><title>Mosaic ring Y chromosome in two normal healthy men with azoospermia</title><title>Fertility and sterility</title><addtitle>Fertil Steril</addtitle><description>To better define by molecular and cytogenetic techniques ring Y chromosomes detected in 2 infertile men.
Case report.
Molecular genetics/cytogenetics unit in a university hospital.
Two infertile men with azoospermia, presenting a normal male phenotype with complete masculinization.
Karyotype and genetic counseling.
Metaphases were studied by standard G- and Q-banding; fluorescent in situ hybridization and PCR were performed to analyze specific Y chromosome regions.
Chromosomal analysis detected a mosaicism with a Y chromosome ring cell line in 92% (patient 1) and 95% (patient 2) of the metaphases, coexisting with a 45,X cell line in the remaining metaphases. In patient 1, PCR analysis showed the presence of AZFa region and a partial deletion of AZFb region; AZFc region was deleted. In patient 2 all three AZF regions were deleted.
A 45,X/46,X,r(Y) mosaicism can be detected not only in patients with Ullrich-Turner syndrome and in patients with various degrees of genital ambiguity but also in men presenting a normal phenotype. Their azoospermia can be explained by partial or total deletion of AZF regions.</description><subject>Adult</subject><subject>AZF regions</subject><subject>Azoospermia</subject><subject>Chromosomes, Human, Y</subject><subject>FISH</subject><subject>Humans</subject><subject>In Situ Hybridization, Fluorescence</subject><subject>infertile male</subject><subject>Male</subject><subject>Mosaicism</subject><subject>Oligospermia - genetics</subject><subject>Ring Chromosomes</subject><subject>ring Y chromosome</subject><subject>Sex Chromosome Aberrations</subject><issn>0015-0282</issn><issn>1556-5653</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkD1PwzAQhi0EouXjLyBPbAlnJ7aTESq-JBALDEyW65ypqyQudkoFv55UrcTIcrc87726hxDKIGfA5NUydxiHPg3jzDmAyEHmUJQHZMqEkJmQojgkUwAmMuAVn5CTlJYAIJnix2TCZCHqWskpmT2HZLyl0fcf9J3aRQxdSKFD6ns6bALtQ-xMSxdo2mHxTTvs6cYPC2p-QkgrjJ03Z-TImTbh-X6fkre729fZQ_b0cv84u37KbFGoMnMlQl0LxdE5peqqUIqVTiErqwZ4yWXlEIS1zdwp0whUYNncMWXsvHFgeXFKLnd3VzF8rjENuvPJYtuaHsM6aVnVwGsJI1jtQBtDShGdXkXfmfitGeitQL3UfwL1VqAGqUeBY_Ri37Ged9j8BffGRuBmB-D46ZfHqJP12FtsfEQ76Cb4_1t-AVCzh-k</recordid><startdate>200512</startdate><enddate>200512</enddate><creator>Bertini, Veronica</creator><creator>Canale, Domenico</creator><creator>Bicocchi, Maria Patrizia</creator><creator>Simi, Paolo</creator><creator>Valetto, Angelo</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>200512</creationdate><title>Mosaic ring Y chromosome in two normal healthy men with azoospermia</title><author>Bertini, Veronica ; Canale, Domenico ; Bicocchi, Maria Patrizia ; Simi, Paolo ; Valetto, Angelo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3374-f4e099572eff779837714f7e148d024268fe05ccdbf7ad5e70c1bf17acbdf0c23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Adult</topic><topic>AZF regions</topic><topic>Azoospermia</topic><topic>Chromosomes, Human, Y</topic><topic>FISH</topic><topic>Humans</topic><topic>In Situ Hybridization, Fluorescence</topic><topic>infertile male</topic><topic>Male</topic><topic>Mosaicism</topic><topic>Oligospermia - genetics</topic><topic>Ring Chromosomes</topic><topic>ring Y chromosome</topic><topic>Sex Chromosome Aberrations</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bertini, Veronica</creatorcontrib><creatorcontrib>Canale, Domenico</creatorcontrib><creatorcontrib>Bicocchi, Maria Patrizia</creatorcontrib><creatorcontrib>Simi, Paolo</creatorcontrib><creatorcontrib>Valetto, Angelo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Fertility and sterility</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bertini, Veronica</au><au>Canale, Domenico</au><au>Bicocchi, Maria Patrizia</au><au>Simi, Paolo</au><au>Valetto, Angelo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mosaic ring Y chromosome in two normal healthy men with azoospermia</atitle><jtitle>Fertility and sterility</jtitle><addtitle>Fertil Steril</addtitle><date>2005-12</date><risdate>2005</risdate><volume>84</volume><issue>6</issue><spage>1744.e1</spage><epage>1744.e4</epage><pages>1744.e1-1744.e4</pages><issn>0015-0282</issn><eissn>1556-5653</eissn><abstract>To better define by molecular and cytogenetic techniques ring Y chromosomes detected in 2 infertile men.
Case report.
Molecular genetics/cytogenetics unit in a university hospital.
Two infertile men with azoospermia, presenting a normal male phenotype with complete masculinization.
Karyotype and genetic counseling.
Metaphases were studied by standard G- and Q-banding; fluorescent in situ hybridization and PCR were performed to analyze specific Y chromosome regions.
Chromosomal analysis detected a mosaicism with a Y chromosome ring cell line in 92% (patient 1) and 95% (patient 2) of the metaphases, coexisting with a 45,X cell line in the remaining metaphases. In patient 1, PCR analysis showed the presence of AZFa region and a partial deletion of AZFb region; AZFc region was deleted. In patient 2 all three AZF regions were deleted.
A 45,X/46,X,r(Y) mosaicism can be detected not only in patients with Ullrich-Turner syndrome and in patients with various degrees of genital ambiguity but also in men presenting a normal phenotype. Their azoospermia can be explained by partial or total deletion of AZF regions.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>16359976</pmid><doi>10.1016/j.fertnstert.2005.06.034</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Elsevier ScienceDirect Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection |
subjects | Adult AZF regions Azoospermia Chromosomes, Human, Y FISH Humans In Situ Hybridization, Fluorescence infertile male Male Mosaicism Oligospermia - genetics Ring Chromosomes ring Y chromosome Sex Chromosome Aberrations |
title | Mosaic ring Y chromosome in two normal healthy men with azoospermia |
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