<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"
	xmlns:content="http://purl.org/rss/1.0/modules/content/"
	xmlns:wfw="http://wellformedweb.org/CommentAPI/"
	xmlns:dc="http://purl.org/dc/elements/1.1/"
	xmlns:atom="http://www.w3.org/2005/Atom"
	xmlns:sy="http://purl.org/rss/1.0/modules/syndication/"
	xmlns:slash="http://purl.org/rss/1.0/modules/slash/"
	>

<channel>
	<title>South Korea Archives - Global NIPT Consortium</title>
	<atom:link href="https://niptconsortium.com/category/south-korea/feed/" rel="self" type="application/rss+xml" />
	<link>https://niptconsortium.com/category/south-korea/</link>
	<description>Noninvasive Prenatal Testing (NIPT) Consortium</description>
	<lastBuildDate>Thu, 30 Nov 2023 16:12:19 +0000</lastBuildDate>
	<language>en-US</language>
	<sy:updatePeriod>
	hourly	</sy:updatePeriod>
	<sy:updateFrequency>
	1	</sy:updateFrequency>
	
	<item>
		<title>Prenatal Diagnosis of Uniparental Disomy in Cases of Rare Autosomal Trisomies Detected Using Noninvasive Prenatal Test: A Case of Prader-Willi Syndrome.</title>
		<link>https://niptconsortium.com/prenatal-diagnosis-of-uniparental-disomy-in-cases-of-rare-autosomal-trisomies-detected-using-noninvasive-prenatal-test-a-case-of-prader-willi-syndrome/</link>
		
		<dc:creator><![CDATA[NIPTadmin]]></dc:creator>
		<pubDate>Thu, 30 Nov 2023 16:12:19 +0000</pubDate>
				<category><![CDATA[2023]]></category>
		<category><![CDATA[Case Report / Case Series]]></category>
		<category><![CDATA[RAAs]]></category>
		<category><![CDATA[South Korea]]></category>
		<guid isPermaLink="false">https://niptconsortium.com/?p=9989</guid>

					<description><![CDATA[<p>Hong DK, Park JE, Kang KM, et al. Diagnostics (Basel). 2023;13(4):580. Published 2023 Feb 4. doi:10.3390/diagnostics13040580. Open Access: Learn more Tags: Case Report / Case Series, 2023, South Korea, RAAs “Overall, six cases were diagnosed with RATs. There was a suspicion of trisomies of chromosomes 7, 8, and 15 in two cases each. However, these [&#8230;]</p>
<p>The post <a href="https://niptconsortium.com/prenatal-diagnosis-of-uniparental-disomy-in-cases-of-rare-autosomal-trisomies-detected-using-noninvasive-prenatal-test-a-case-of-prader-willi-syndrome/">Prenatal Diagnosis of Uniparental Disomy in Cases of Rare Autosomal Trisomies Detected Using Noninvasive Prenatal Test: A Case of Prader-Willi Syndrome.</a> appeared first on <a href="https://niptconsortium.com">Global NIPT Consortium</a>.</p>
]]></description>
										<content:encoded><![CDATA[<p>Hong DK, Park JE, Kang KM, et al. <em>Diagnostics (Basel).</em> 2023;13(4):580. Published 2023 Feb 4. doi:10.3390/diagnostics13040580. Open Access: <a href="https://www.mdpi.com/2075-4418/13/4/580" target="_blank" rel="noopener">Learn more</a></p>
<p><strong><em>Tags:</em></strong><em> Case Report / Case Series, 2023, South Korea, RAAs </em></p>
<ul>
<li>“Overall, six cases were diagnosed with RATs. There was a suspicion of trisomies of chromosomes 7, 8, and 15 in two cases each. However, these cases were confirmed to have a normal karyotype using amniocentesis. In one of six cases, PWS [Prader-Willi syndrome] caused by maternal UPD 15 was diagnosed using MS-PCR and MS-MLPA. We propose that in cases where RAT is detected by NIPT, UPD should be considered following trisomy rescue. Even if amniocentesis confirms a normal karyotype, UPD testing (such as MS-PCR and MS-MLPA) should be recommended for accurate assessment, as an accurate diagnosis can lead to appropriate genetic counseling and improved overall pregnancy management.”</li>
</ul>
<p>The post <a href="https://niptconsortium.com/prenatal-diagnosis-of-uniparental-disomy-in-cases-of-rare-autosomal-trisomies-detected-using-noninvasive-prenatal-test-a-case-of-prader-willi-syndrome/">Prenatal Diagnosis of Uniparental Disomy in Cases of Rare Autosomal Trisomies Detected Using Noninvasive Prenatal Test: A Case of Prader-Willi Syndrome.</a> appeared first on <a href="https://niptconsortium.com">Global NIPT Consortium</a>.</p>
]]></content:encoded>
					
		
		
			</item>
	</channel>
</rss>
