Trisomic 22 placenta in a case of severe intrauterine growth retardation
We describe a case in which a trisomic 22 placenta could be the cause of severe growth retardation in a chromosomally normal female fetus. At amniocentesis a mosaic 46,XX/ 47,XX, +22 was observed in amniotic fluid specimens sampled on two different occasions, while fetal blood from a diagnostic cord...
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| Veröffentlicht in: | Prenatal diagnosis 1989-09, Vol.9 (9), p.673-676 |
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| container_end_page | 676 |
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| container_issue | 9 |
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| container_title | Prenatal diagnosis |
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| creator | Stioui, S. de Silvestris, M. Molinari, A. Stripparo, L. Ghisoni, L. Simoni, G. |
| description | We describe a case in which a trisomic 22 placenta could be the cause of severe growth retardation in a chromosomally normal female fetus. At amniocentesis a mosaic 46,XX/ 47,XX, +22 was observed in amniotic fluid specimens sampled on two different occasions, while fetal blood from a diagnostic cordocentesis revealed a normal chromosome constitution. Postnatal studies showed the consistent presence of trisomic 22 cells in the placenta, while only normal metaphases were found in amnion, blood, and fibroblast cultures. |
| doi_str_mv | 10.1002/pd.1970090911 |
| format | Article |
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At amniocentesis a mosaic 46,XX/ 47,XX, +22 was observed in amniotic fluid specimens sampled on two different occasions, while fetal blood from a diagnostic cordocentesis revealed a normal chromosome constitution. Postnatal studies showed the consistent presence of trisomic 22 cells in the placenta, while only normal metaphases were found in amnion, blood, and fibroblast cultures.</description><identifier>ISSN: 0197-3851</identifier><identifier>EISSN: 1097-0223</identifier><identifier>DOI: 10.1002/pd.1970090911</identifier><identifier>PMID: 2798352</identifier><identifier>CODEN: PRDIDM</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>Biological and medical sciences ; Chorionic villi ; Chorionic Villi - ultrastructure ; Chromosomal mosaicism ; Chromosomes, Human, Pair 22 ; Female ; Fetal Growth Retardation - etiology ; Gynecology. Andrology. Obstetrics ; Humans ; Intrauterine growth retardation ; Karyotyping ; Management. 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Diagn</addtitle><description>We describe a case in which a trisomic 22 placenta could be the cause of severe growth retardation in a chromosomally normal female fetus. At amniocentesis a mosaic 46,XX/ 47,XX, +22 was observed in amniotic fluid specimens sampled on two different occasions, while fetal blood from a diagnostic cordocentesis revealed a normal chromosome constitution. Postnatal studies showed the consistent presence of trisomic 22 cells in the placenta, while only normal metaphases were found in amnion, blood, and fibroblast cultures.</description><subject>Biological and medical sciences</subject><subject>Chorionic villi</subject><subject>Chorionic Villi - ultrastructure</subject><subject>Chromosomal mosaicism</subject><subject>Chromosomes, Human, Pair 22</subject><subject>Female</subject><subject>Fetal Growth Retardation - etiology</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>Intrauterine growth retardation</subject><subject>Karyotyping</subject><subject>Management. Prenatal diagnosis</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Mosaicism</subject><subject>Placenta Diseases - complications</subject><subject>Placenta Diseases - genetics</subject><subject>Pregnancy</subject><subject>Pregnancy. Fetus. Placenta</subject><subject>Trisomy</subject><subject>Trisomy 22</subject><issn>0197-3851</issn><issn>1097-0223</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkM1P3DAQxa2KChbaI0ckH1BvAX_EcXxE0C6VllKpW3G0Js4YDNkk2NkC_31TbbQVFziNNO83b54eIYecnXDGxGlfn3CjGTPMcP6BzDgzOmNCyB0yY6OSyVLxPbKf0v2Il8LoXbIrtCmlEjNyuYwhdavgqBC0b8BhOwANLQXqICHtPE34ByOOuyHCesAYWqS3sXsa7mjEAWINQ-jaT-Sjhybh52kekN_fvi7PL7PF9fz7-dkic7nMeaZVZepCeqmUhzI3SuXOFxVHVFoXzHFfaKiML72p69wr8AVwFCCAiaouuTwgXza-fewe15gGuwrJYdNAi906WW2EYjLX74J8fMglUyOYbUAXu5QietvHsIL4Yjmz_yq2fW3_VzzyR5PxulphvaWnTkf9eNIhOWh8hNaFtMUKI7Uu8xHTG-wpNPjy9k_78-JVgClwSAM-by8hPthCS63szY-5VYtfC17eXNml_AvARaIA</recordid><startdate>198909</startdate><enddate>198909</enddate><creator>Stioui, S.</creator><creator>de Silvestris, M.</creator><creator>Molinari, A.</creator><creator>Stripparo, L.</creator><creator>Ghisoni, L.</creator><creator>Simoni, G.</creator><general>John Wiley & Sons, Ltd</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</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>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>198909</creationdate><title>Trisomic 22 placenta in a case of severe intrauterine growth retardation</title><author>Stioui, S. ; de Silvestris, M. ; Molinari, A. ; Stripparo, L. ; Ghisoni, L. ; Simoni, G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4341-75b9d63f355fa849554cf6b1ee57760c1f67ab9f8f9dd4f5af6a1e2a2a02bd813</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Biological and medical sciences</topic><topic>Chorionic villi</topic><topic>Chorionic Villi - ultrastructure</topic><topic>Chromosomal mosaicism</topic><topic>Chromosomes, Human, Pair 22</topic><topic>Female</topic><topic>Fetal Growth Retardation - etiology</topic><topic>Gynecology. 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Placenta</topic><topic>Trisomy</topic><topic>Trisomy 22</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stioui, S.</creatorcontrib><creatorcontrib>de Silvestris, M.</creatorcontrib><creatorcontrib>Molinari, A.</creatorcontrib><creatorcontrib>Stripparo, L.</creatorcontrib><creatorcontrib>Ghisoni, L.</creatorcontrib><creatorcontrib>Simoni, G.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Prenatal diagnosis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stioui, S.</au><au>de Silvestris, M.</au><au>Molinari, A.</au><au>Stripparo, L.</au><au>Ghisoni, L.</au><au>Simoni, G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Trisomic 22 placenta in a case of severe intrauterine growth retardation</atitle><jtitle>Prenatal diagnosis</jtitle><addtitle>Prenat. Diagn</addtitle><date>1989-09</date><risdate>1989</risdate><volume>9</volume><issue>9</issue><spage>673</spage><epage>676</epage><pages>673-676</pages><issn>0197-3851</issn><eissn>1097-0223</eissn><coden>PRDIDM</coden><abstract>We describe a case in which a trisomic 22 placenta could be the cause of severe growth retardation in a chromosomally normal female fetus. At amniocentesis a mosaic 46,XX/ 47,XX, +22 was observed in amniotic fluid specimens sampled on two different occasions, while fetal blood from a diagnostic cordocentesis revealed a normal chromosome constitution. Postnatal studies showed the consistent presence of trisomic 22 cells in the placenta, while only normal metaphases were found in amnion, blood, and fibroblast cultures.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>2798352</pmid><doi>10.1002/pd.1970090911</doi><tpages>4</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0197-3851 |
| ispartof | Prenatal diagnosis, 1989-09, Vol.9 (9), p.673-676 |
| issn | 0197-3851 1097-0223 |
| language | eng |
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| source | MEDLINE; Wiley Journals |
| subjects | Biological and medical sciences Chorionic villi Chorionic Villi - ultrastructure Chromosomal mosaicism Chromosomes, Human, Pair 22 Female Fetal Growth Retardation - etiology Gynecology. Andrology. Obstetrics Humans Intrauterine growth retardation Karyotyping Management. Prenatal diagnosis Medical sciences Middle Aged Mosaicism Placenta Diseases - complications Placenta Diseases - genetics Pregnancy Pregnancy. Fetus. Placenta Trisomy Trisomy 22 |
| title | Trisomic 22 placenta in a case of severe intrauterine growth retardation |
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