An uncommon complementary isochromosome of 46,XY, i(9)(p10),i(9)(q10) in an infertile oligoasthenoteratozoospermic man
Objective To report a rare case of male infertility associated with oligoasthenoteratozoospermia and complementary isochromosome 46 XY, i(9)(p10),i(9)(q10). Design Case report. Setting Reference hospital. Patient(s) Infertile oligoastenozoospermic man with complementary isochromosome 46,XY, i(9)(p10...
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| Veröffentlicht in: | Fertility and sterility 2011, Vol.95 (1), p.290.e5-290.e8 |
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| creator | Guvendag Guven, Emine Seda, M.D Dilbaz, Serdar, M.D Ceylaner, Serdar, M.D Acar, Hasan, M.D Cinar, Ozgur, M.D Ozdegirmenci, Ozlem, M.D Karcaaltincaba, Deniz, M.D |
| description | Objective To report a rare case of male infertility associated with oligoasthenoteratozoospermia and complementary isochromosome 46 XY, i(9)(p10),i(9)(q10). Design Case report. Setting Reference hospital. Patient(s) Infertile oligoastenozoospermic man with complementary isochromosome 46,XY, i(9)(p10),i(9)(q10). Intervention(s) Peripheral blood lymphocytes obtained for karyotyping, and florescence in situ hybridization (FISH) analysis for gonadal mosaicism in ejaculated spermatozoa. Main Outcome Measure(s) Physical examination, semen analysis, GBG banding, and FISH procedure. Result(s) The semen analysis revealed oligoasthenoteratozoospermia. The lymphocytic karyotype detected a complementary isochromosome 46,XY, i(9)(p10),i(9)(q10), and the FISH procedure showed abnormal sperm. Conclusion(s) This the first report of oligoasthenoteratozoospermia associated with complementary isochromosome 46,XY, i(9)(p10),i(9)(q10). |
| doi_str_mv | 10.1016/j.fertnstert.2010.05.028 |
| format | Article |
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Design Case report. Setting Reference hospital. Patient(s) Infertile oligoastenozoospermic man with complementary isochromosome 46,XY, i(9)(p10),i(9)(q10). Intervention(s) Peripheral blood lymphocytes obtained for karyotyping, and florescence in situ hybridization (FISH) analysis for gonadal mosaicism in ejaculated spermatozoa. Main Outcome Measure(s) Physical examination, semen analysis, GBG banding, and FISH procedure. Result(s) The semen analysis revealed oligoasthenoteratozoospermia. The lymphocytic karyotype detected a complementary isochromosome 46,XY, i(9)(p10),i(9)(q10), and the FISH procedure showed abnormal sperm. Conclusion(s) This the first report of oligoasthenoteratozoospermia associated with complementary isochromosome 46,XY, i(9)(p10),i(9)(q10).</description><identifier>ISSN: 0015-0282</identifier><identifier>EISSN: 1556-5653</identifier><identifier>DOI: 10.1016/j.fertnstert.2010.05.028</identifier><identifier>PMID: 20646692</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Asthenozoospermia - genetics ; Azoospermia ; case studies ; Chromosome Banding ; Chromosomes, Human, Pair 9 ; clinical examination ; Female ; fluorescence in situ hybridization ; Humans ; Infertility, Male - genetics ; Internal Medicine ; isochromosome ; Isochromosomes ; karyotyping ; lymphocytes ; Male ; male fertility ; male infertility ; nonrobertsonian translocation ; Obstetrics and Gynecology ; Oligospermia - genetics ; patients ; semen ; spermatozoa ; Translocation, Genetic - genetics</subject><ispartof>Fertility and sterility, 2011, Vol.95 (1), p.290.e5-290.e8</ispartof><rights>American Society for Reproductive Medicine</rights><rights>2011 American Society for Reproductive Medicine</rights><rights>Copyright © 2011 American Society for Reproductive Medicine. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c447t-45abd0fe2064f18cfec8288af7f1506f9a181607ad417c8183ce718ea38ee8263</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.fertnstert.2010.05.028$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,4024,27923,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20646692$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Guvendag Guven, Emine Seda, M.D</creatorcontrib><creatorcontrib>Dilbaz, Serdar, M.D</creatorcontrib><creatorcontrib>Ceylaner, Serdar, M.D</creatorcontrib><creatorcontrib>Acar, Hasan, M.D</creatorcontrib><creatorcontrib>Cinar, Ozgur, M.D</creatorcontrib><creatorcontrib>Ozdegirmenci, Ozlem, M.D</creatorcontrib><creatorcontrib>Karcaaltincaba, Deniz, M.D</creatorcontrib><title>An uncommon complementary isochromosome of 46,XY, i(9)(p10),i(9)(q10) in an infertile oligoasthenoteratozoospermic man</title><title>Fertility and sterility</title><addtitle>Fertil Steril</addtitle><description>Objective To report a rare case of male infertility associated with oligoasthenoteratozoospermia and complementary isochromosome 46 XY, i(9)(p10),i(9)(q10). Design Case report. Setting Reference hospital. Patient(s) Infertile oligoastenozoospermic man with complementary isochromosome 46,XY, i(9)(p10),i(9)(q10). Intervention(s) Peripheral blood lymphocytes obtained for karyotyping, and florescence in situ hybridization (FISH) analysis for gonadal mosaicism in ejaculated spermatozoa. Main Outcome Measure(s) Physical examination, semen analysis, GBG banding, and FISH procedure. Result(s) The semen analysis revealed oligoasthenoteratozoospermia. The lymphocytic karyotype detected a complementary isochromosome 46,XY, i(9)(p10),i(9)(q10), and the FISH procedure showed abnormal sperm. Conclusion(s) This the first report of oligoasthenoteratozoospermia associated with complementary isochromosome 46,XY, i(9)(p10),i(9)(q10).</description><subject>Adult</subject><subject>Asthenozoospermia - genetics</subject><subject>Azoospermia</subject><subject>case studies</subject><subject>Chromosome Banding</subject><subject>Chromosomes, Human, Pair 9</subject><subject>clinical examination</subject><subject>Female</subject><subject>fluorescence in situ hybridization</subject><subject>Humans</subject><subject>Infertility, Male - genetics</subject><subject>Internal Medicine</subject><subject>isochromosome</subject><subject>Isochromosomes</subject><subject>karyotyping</subject><subject>lymphocytes</subject><subject>Male</subject><subject>male fertility</subject><subject>male infertility</subject><subject>nonrobertsonian translocation</subject><subject>Obstetrics and Gynecology</subject><subject>Oligospermia - genetics</subject><subject>patients</subject><subject>semen</subject><subject>spermatozoa</subject><subject>Translocation, Genetic - genetics</subject><issn>0015-0282</issn><issn>1556-5653</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkk1v1DAQhi0EokvLXwDfaKXNYjux41wqlYqPSpU4tJXgZLnOuPUS26mdVCq_HoctIPXEZWY0emf86vEghCnZUELF--3GQppCnkrcMFLahG8Ik8_QinIuKi54_RytCKG8Km22h17lvCWECNqyl2iPEdEI0bEVuj8JeA4meh8DLmkcwEOYdHrALkdzm6KPOXrA0eJGrL99X2N32B0djpQcrX9Xd6XCLmAdSlxsuaGoB3cTdZ5uIcRiUk_xZ4x5hOSdwV6HA_TC6iHD68e8j64-fbw8_VKdf_18dnpyXpmmaaeq4fq6JxYWv5ZKY8FIJqW2raWcCNtpKqkgre4b2hpJZW2gpRJ0LQEkE_U-erfbO6Z4N0OelHfZwDDoAHHOSjLSyo51bVHKndKkmHMCq8bkfOGgKFELdLVV_6CrBboiXBW6ZfTN4yPztYf-7-AfykXwdiewOip9k1xWVxdlAy8fxFomlhUfdgooMO4dJJWNg2CgdwnMpPro_sfH8ZMlZnDBGT38gAfI2zinUGArqjJTRF0s57FcBy2HUdiJ-hd4SbYN</recordid><startdate>2011</startdate><enddate>2011</enddate><creator>Guvendag Guven, Emine Seda, M.D</creator><creator>Dilbaz, Serdar, M.D</creator><creator>Ceylaner, Serdar, M.D</creator><creator>Acar, Hasan, M.D</creator><creator>Cinar, Ozgur, M.D</creator><creator>Ozdegirmenci, Ozlem, M.D</creator><creator>Karcaaltincaba, Deniz, M.D</creator><general>Elsevier Inc</general><scope>FBQ</scope><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>2011</creationdate><title>An uncommon complementary isochromosome of 46,XY, i(9)(p10),i(9)(q10) in an infertile oligoasthenoteratozoospermic man</title><author>Guvendag Guven, Emine Seda, M.D ; Dilbaz, Serdar, M.D ; Ceylaner, Serdar, M.D ; Acar, Hasan, M.D ; Cinar, Ozgur, M.D ; Ozdegirmenci, Ozlem, M.D ; Karcaaltincaba, Deniz, M.D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c447t-45abd0fe2064f18cfec8288af7f1506f9a181607ad417c8183ce718ea38ee8263</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adult</topic><topic>Asthenozoospermia - genetics</topic><topic>Azoospermia</topic><topic>case studies</topic><topic>Chromosome Banding</topic><topic>Chromosomes, Human, Pair 9</topic><topic>clinical examination</topic><topic>Female</topic><topic>fluorescence in situ hybridization</topic><topic>Humans</topic><topic>Infertility, Male - genetics</topic><topic>Internal Medicine</topic><topic>isochromosome</topic><topic>Isochromosomes</topic><topic>karyotyping</topic><topic>lymphocytes</topic><topic>Male</topic><topic>male fertility</topic><topic>male infertility</topic><topic>nonrobertsonian translocation</topic><topic>Obstetrics and Gynecology</topic><topic>Oligospermia - genetics</topic><topic>patients</topic><topic>semen</topic><topic>spermatozoa</topic><topic>Translocation, Genetic - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Guvendag Guven, Emine Seda, M.D</creatorcontrib><creatorcontrib>Dilbaz, Serdar, M.D</creatorcontrib><creatorcontrib>Ceylaner, Serdar, M.D</creatorcontrib><creatorcontrib>Acar, Hasan, M.D</creatorcontrib><creatorcontrib>Cinar, Ozgur, M.D</creatorcontrib><creatorcontrib>Ozdegirmenci, Ozlem, M.D</creatorcontrib><creatorcontrib>Karcaaltincaba, Deniz, M.D</creatorcontrib><collection>AGRIS</collection><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>Guvendag Guven, Emine Seda, M.D</au><au>Dilbaz, Serdar, M.D</au><au>Ceylaner, Serdar, M.D</au><au>Acar, Hasan, M.D</au><au>Cinar, Ozgur, M.D</au><au>Ozdegirmenci, Ozlem, M.D</au><au>Karcaaltincaba, Deniz, M.D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An uncommon complementary isochromosome of 46,XY, i(9)(p10),i(9)(q10) in an infertile oligoasthenoteratozoospermic man</atitle><jtitle>Fertility and sterility</jtitle><addtitle>Fertil Steril</addtitle><date>2011</date><risdate>2011</risdate><volume>95</volume><issue>1</issue><spage>290.e5</spage><epage>290.e8</epage><pages>290.e5-290.e8</pages><issn>0015-0282</issn><eissn>1556-5653</eissn><abstract>Objective To report a rare case of male infertility associated with oligoasthenoteratozoospermia and complementary isochromosome 46 XY, i(9)(p10),i(9)(q10). Design Case report. Setting Reference hospital. Patient(s) Infertile oligoastenozoospermic man with complementary isochromosome 46,XY, i(9)(p10),i(9)(q10). Intervention(s) Peripheral blood lymphocytes obtained for karyotyping, and florescence in situ hybridization (FISH) analysis for gonadal mosaicism in ejaculated spermatozoa. Main Outcome Measure(s) Physical examination, semen analysis, GBG banding, and FISH procedure. Result(s) The semen analysis revealed oligoasthenoteratozoospermia. The lymphocytic karyotype detected a complementary isochromosome 46,XY, i(9)(p10),i(9)(q10), and the FISH procedure showed abnormal sperm. Conclusion(s) This the first report of oligoasthenoteratozoospermia associated with complementary isochromosome 46,XY, i(9)(p10),i(9)(q10).</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>20646692</pmid><doi>10.1016/j.fertnstert.2010.05.028</doi><oa>free_for_read</oa></addata></record> |
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| ispartof | Fertility and sterility, 2011, Vol.95 (1), p.290.e5-290.e8 |
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| source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; ScienceDirect Journals (5 years ago - present); Alma/SFX Local Collection |
| subjects | Adult Asthenozoospermia - genetics Azoospermia case studies Chromosome Banding Chromosomes, Human, Pair 9 clinical examination Female fluorescence in situ hybridization Humans Infertility, Male - genetics Internal Medicine isochromosome Isochromosomes karyotyping lymphocytes Male male fertility male infertility nonrobertsonian translocation Obstetrics and Gynecology Oligospermia - genetics patients semen spermatozoa Translocation, Genetic - genetics |
| title | An uncommon complementary isochromosome of 46,XY, i(9)(p10),i(9)(q10) in an infertile oligoasthenoteratozoospermic man |
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