Increasing prenatal diagnosis of chimeras with the use of noninvasive prenatal screening: Report of two cases
Bulleted Statements: What's already known about this topic? The incidence of discordant fetal sex was estimated to be 1 in 1500–2000. Comprehensive evaluation is required to investigate the underlying cause. What does this study add? Chimera is one of the possible causes of genotype–phenotype s...
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| Veröffentlicht in: | Prenatal diagnosis 2021-05, Vol.41 (6), p.697-700 |
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| container_end_page | 700 |
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| container_issue | 6 |
| container_start_page | 697 |
| container_title | Prenatal diagnosis |
| container_volume | 41 |
| creator | Yu, Florrie N. Y. Li, Elizabeth Y. Y. Kong, Meliza C. W. Ma, Teresa W. L. Chan, Kelvin Y. K. Man, Elim Chung, Brian H. Y. Kan, Anita S. Y. |
| description | Bulleted Statements:
What's already known about this topic?
The incidence of discordant fetal sex was estimated to be 1 in 1500–2000. Comprehensive evaluation is required to investigate the underlying cause.
What does this study add?
Chimera is one of the possible causes of genotype–phenotype sex discordance. It could be detected prenatally with the combination of noninvasive prenatal screening and ultrasound.
Genetic counseling to prospective parents on chimera can be complex where early support and information from experienced professionals are important. |
| doi_str_mv | 10.1002/pd.5911 |
| format | Article |
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What's already known about this topic?
The incidence of discordant fetal sex was estimated to be 1 in 1500–2000. Comprehensive evaluation is required to investigate the underlying cause.
What does this study add?
Chimera is one of the possible causes of genotype–phenotype sex discordance. It could be detected prenatally with the combination of noninvasive prenatal screening and ultrasound.
Genetic counseling to prospective parents on chimera can be complex where early support and information from experienced professionals are important.</description><identifier>ISSN: 0197-3851</identifier><identifier>EISSN: 1097-0223</identifier><identifier>DOI: 10.1002/pd.5911</identifier><identifier>PMID: 33527400</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Adult ; Chimera - genetics ; Chimeras ; Female ; Humans ; Medical diagnosis ; Noninvasive Prenatal Testing - methods ; Noninvasive Prenatal Testing - statistics & numerical data ; Pregnancy ; Prenatal diagnosis</subject><ispartof>Prenatal diagnosis, 2021-05, Vol.41 (6), p.697-700</ispartof><rights>2021 John Wiley & Sons Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3071-5f4abe3bffd07852171174f8ac711d8057842028d3528a78f0cab91a154d41ac3</cites><orcidid>0000-0003-4922-434X ; 0000-0001-7379-003X ; 0000-0002-7044-5916</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fpd.5911$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fpd.5911$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33527400$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yu, Florrie N. Y.</creatorcontrib><creatorcontrib>Li, Elizabeth Y. Y.</creatorcontrib><creatorcontrib>Kong, Meliza C. W.</creatorcontrib><creatorcontrib>Ma, Teresa W. L.</creatorcontrib><creatorcontrib>Chan, Kelvin Y. K.</creatorcontrib><creatorcontrib>Man, Elim</creatorcontrib><creatorcontrib>Chung, Brian H. Y.</creatorcontrib><creatorcontrib>Kan, Anita S. Y.</creatorcontrib><title>Increasing prenatal diagnosis of chimeras with the use of noninvasive prenatal screening: Report of two cases</title><title>Prenatal diagnosis</title><addtitle>Prenat Diagn</addtitle><description>Bulleted Statements:
What's already known about this topic?
The incidence of discordant fetal sex was estimated to be 1 in 1500–2000. Comprehensive evaluation is required to investigate the underlying cause.
What does this study add?
Chimera is one of the possible causes of genotype–phenotype sex discordance. It could be detected prenatally with the combination of noninvasive prenatal screening and ultrasound.
Genetic counseling to prospective parents on chimera can be complex where early support and information from experienced professionals are important.</description><subject>Adult</subject><subject>Chimera - genetics</subject><subject>Chimeras</subject><subject>Female</subject><subject>Humans</subject><subject>Medical diagnosis</subject><subject>Noninvasive Prenatal Testing - methods</subject><subject>Noninvasive Prenatal Testing - statistics & numerical data</subject><subject>Pregnancy</subject><subject>Prenatal diagnosis</subject><issn>0197-3851</issn><issn>1097-0223</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kdtKxDAQQIMoul7wDyTgg4KsJmljUt9kvYKgiD6HbDrdjbRJTVoX_97U9QKCTzNMzhwyMwjtUnJMCWEnbXnMC0pX0IiSQowJY9kqGhGa8kxyuoE2Y3xJoGSFWEcbWcaZyAkZoebWmQA6WjfDbQCnO13j0uqZ89FG7Cts5raBoCNe2G6OuzngPsLw4Lyz7i21vsFva0w2SPXZGX6E1oduILuFx0ZHiNtordJ1hJ2vuIWery6fJjfju_vr28n53dhkRNAxr3I9hWxaVSURkjMqKBV5JbVJSSkJFzJnaZgyjSG1kBUxelpQTXle5lSbbAsdLr1t8K89xE41Nhqoa-3A91GxXHJOecFOE7r_B33xfXDpd4oNS5JCMpmogyVlgo8xQKXaYBsd3hUlariAaks1XCCRe1--ftpA-cN9rzwBR0tgYWt4_8-jHi4-dR-WLo3P</recordid><startdate>202105</startdate><enddate>202105</enddate><creator>Yu, Florrie N. 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Y.</au><au>Li, Elizabeth Y. Y.</au><au>Kong, Meliza C. W.</au><au>Ma, Teresa W. L.</au><au>Chan, Kelvin Y. K.</au><au>Man, Elim</au><au>Chung, Brian H. Y.</au><au>Kan, Anita S. Y.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Increasing prenatal diagnosis of chimeras with the use of noninvasive prenatal screening: Report of two cases</atitle><jtitle>Prenatal diagnosis</jtitle><addtitle>Prenat Diagn</addtitle><date>2021-05</date><risdate>2021</risdate><volume>41</volume><issue>6</issue><spage>697</spage><epage>700</epage><pages>697-700</pages><issn>0197-3851</issn><eissn>1097-0223</eissn><abstract>Bulleted Statements:
What's already known about this topic?
The incidence of discordant fetal sex was estimated to be 1 in 1500–2000. Comprehensive evaluation is required to investigate the underlying cause.
What does this study add?
Chimera is one of the possible causes of genotype–phenotype sex discordance. It could be detected prenatally with the combination of noninvasive prenatal screening and ultrasound.
Genetic counseling to prospective parents on chimera can be complex where early support and information from experienced professionals are important.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>33527400</pmid><doi>10.1002/pd.5911</doi><tpages>4</tpages><orcidid>https://orcid.org/0000-0003-4922-434X</orcidid><orcidid>https://orcid.org/0000-0001-7379-003X</orcidid><orcidid>https://orcid.org/0000-0002-7044-5916</orcidid></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0197-3851 |
| ispartof | Prenatal diagnosis, 2021-05, Vol.41 (6), p.697-700 |
| issn | 0197-3851 1097-0223 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_2485515926 |
| source | MEDLINE; Wiley Online Library Journals Frontfile Complete |
| subjects | Adult Chimera - genetics Chimeras Female Humans Medical diagnosis Noninvasive Prenatal Testing - methods Noninvasive Prenatal Testing - statistics & numerical data Pregnancy Prenatal diagnosis |
| title | Increasing prenatal diagnosis of chimeras with the use of noninvasive prenatal screening: Report of two cases |
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