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	<title>Japan Archives - Global NIPT Consortium</title>
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		<title>Confined placental mosaicism of trisomy 6 detected through genome-wide NIPT was associated with placental abruption.</title>
		<link>https://niptconsortium.com/confined-placental-mosaicism-of-trisomy-6-detected-through-genome-wide-nipt-was-associated-with-placental-abruption/</link>
		
		<dc:creator><![CDATA[NIPTadmin]]></dc:creator>
		<pubDate>Tue, 30 Nov 2021 17:26:17 +0000</pubDate>
				<category><![CDATA[2021]]></category>
		<category><![CDATA[Case Report / Case Series]]></category>
		<category><![CDATA[Japan]]></category>
		<category><![CDATA[RAAs]]></category>
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					<description><![CDATA[<p>Nishiyama M, Wada S, Hasegawa F, et al. Clin Case Rep. 2021;9(12):e05155. Published 2021 Dec 5. doi:10.1002/ccr3.5155. Open Access: Learn more Tags: Case Report, 2021, Japan, RAAs Case report of a pregnancy with a NIPT result positive for trisomy 6 and placental abruption.</p>
<p>The post <a href="https://niptconsortium.com/confined-placental-mosaicism-of-trisomy-6-detected-through-genome-wide-nipt-was-associated-with-placental-abruption/">Confined placental mosaicism of trisomy 6 detected through genome-wide NIPT was associated with placental abruption.</a> appeared first on <a href="https://niptconsortium.com">Global NIPT Consortium</a>.</p>
]]></description>
										<content:encoded><![CDATA[<p>Nishiyama M, Wada S, Hasegawa F, et al. <em>Clin Case Rep.</em> 2021;9(12):e05155. Published 2021 Dec 5. doi:10.1002/ccr3.5155. Open Access: <a href="https://onlinelibrary.wiley.com/doi/10.1002/ccr3.5155" target="_blank" rel="noopener">Learn more</a></p>
<p><strong><em>Tags:</em></strong><em> Case Report, 2021, Japan, RAAs</em></p>
<ul>
<li>Case report of a pregnancy with a NIPT result positive for trisomy 6 and placental abruption.</li>
</ul>
<p>The post <a href="https://niptconsortium.com/confined-placental-mosaicism-of-trisomy-6-detected-through-genome-wide-nipt-was-associated-with-placental-abruption/">Confined placental mosaicism of trisomy 6 detected through genome-wide NIPT was associated with placental abruption.</a> appeared first on <a href="https://niptconsortium.com">Global NIPT Consortium</a>.</p>
]]></content:encoded>
					
		
		
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		<title>Prenatal Identification of Confined Placental Mosaicism in Pregnant Women with Fetal Growth Restriction.</title>
		<link>https://niptconsortium.com/prenatal-identification-of-confined-placental-mosaicism-in-pregnant-women-with-fetal-growth-restriction/</link>
		
		<dc:creator><![CDATA[NIPTadmin]]></dc:creator>
		<pubDate>Tue, 30 Nov 2021 16:47:04 +0000</pubDate>
				<category><![CDATA[2021]]></category>
		<category><![CDATA[Clinical Experience / Clinical Utility]]></category>
		<category><![CDATA[Japan]]></category>
		<category><![CDATA[RAAs]]></category>
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					<description><![CDATA[<p>Miyagami K, Shirato N, Izumi M, et al. Reprod Sci. 2022;29(3):896-903. doi:10.1007/s43032-021-00772-3. Tags: Clinical Experience / Clinical Utility, 2021, Japan, RAAs “cfDNA analyses of maternal plasma detected suspected CPM cases with chromosomal aneuploidy or copy number variations in 5 of 40 cases (12.5%). For 4 cases in which the entire placenta consisted of cells with [&#8230;]</p>
<p>The post <a href="https://niptconsortium.com/prenatal-identification-of-confined-placental-mosaicism-in-pregnant-women-with-fetal-growth-restriction/">Prenatal Identification of Confined Placental Mosaicism in Pregnant Women with Fetal Growth Restriction.</a> appeared first on <a href="https://niptconsortium.com">Global NIPT Consortium</a>.</p>
]]></description>
										<content:encoded><![CDATA[<p>Miyagami K, Shirato N, Izumi M, et al. <em>Reprod Sci.</em> 2022;29(3):896-903. doi:10.1007/s43032-021-00772-3.</p>
<p><strong><em>Tags:</em></strong><em> Clinical Experience / Clinical Utility, 2021, Japan, RAAs</em></p>
<ul>
<li>“cfDNA analyses of maternal plasma detected suspected CPM cases with chromosomal aneuploidy or copy number variations in 5 of 40 cases (12.5%). For 4 cases in which the entire placenta consisted of cells with chromosomal abnormalities, fetal growth was severely restricted. CPM can be screened by cfDNA analysis in maternal plasma, accounting for approximately 10% of the causes of moderate or severe FGR [fetal growth restriction], and the higher the proportion of abnormal karyotype cells in the placenta, the more severe the placental dysfunction and FGR.”</li>
</ul>
<p>The post <a href="https://niptconsortium.com/prenatal-identification-of-confined-placental-mosaicism-in-pregnant-women-with-fetal-growth-restriction/">Prenatal Identification of Confined Placental Mosaicism in Pregnant Women with Fetal Growth Restriction.</a> appeared first on <a href="https://niptconsortium.com">Global NIPT Consortium</a>.</p>
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