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	<title>non-invasive prenatal screening &#8211; BIOENGINEER.ORG</title>
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		<title>Rare Chromosome 15 Duplication Syndrome Often Evades Prenatal Detection, Case Analysis Reveals</title>
		<link>https://bioengineer.org/rare-chromosome-15-duplication-syndrome-often-evades-prenatal-detection-case-analysis-reveals/</link>
		
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		<pubDate>Fri, 16 Oct 2026 19:28:39 +0000</pubDate>
				<category><![CDATA[Health]]></category>
		<category><![CDATA[15q duplication syndrome]]></category>
		<category><![CDATA[chromosome 15q11.2-q13.1]]></category>
		<category><![CDATA[copy number variation]]></category>
		<category><![CDATA[Dup15q syndrome]]></category>
		<category><![CDATA[fetal growth restriction]]></category>
		<category><![CDATA[genetic counseling]]></category>
		<category><![CDATA[neurodevelopmental disorder]]></category>
		<category><![CDATA[non-invasive prenatal screening]]></category>
		<category><![CDATA[polyhydramnios]]></category>
		<category><![CDATA[prenatal diagnosis]]></category>
		<category><![CDATA[UBE3A]]></category>
		<category><![CDATA[whole-exome sequencing]]></category>
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					<description><![CDATA[A new case report and pooled analysis of 35 prenatal cases shows that 15q duplication syndrome frequently escapes prenatal detection because its ultrasound findings are nonspecific, underscoring the value of genetic screening when fetal growth restriction or polyhydramnios appears.]]></description>
		
		
		
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