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		<title>Hutchinson–Gilford Progeria Syndrome</title>
		<link>https://www.laboratorynotes.com/hutchinson-gilford-progeria-syndrome/</link>
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		<pubDate>Sat, 22 Aug 2026 17:38:44 +0000</pubDate>
				<category><![CDATA[Database]]></category>
		<category><![CDATA[Database: Disease]]></category>
		<category><![CDATA[Ageing]]></category>
		<category><![CDATA[Disease]]></category>
		<category><![CDATA[Genomic instability]]></category>
		<category><![CDATA[Hutchinson–Gilford progeria syndrome]]></category>
		<guid isPermaLink="false">https://www.laboratorynotes.com/?p=29762</guid>

					<description><![CDATA[<p>Hutchinson–Gilford progeria syndrome is a rare genetic disorder caused by LMNA mutations that generate progerin, a toxic protein disrupting nuclear structure and accelerating ageing. Children develop rapid cardiovascular decline, growth failure and systemic tissue deterioration, making HGPS one of the most important models for understanding human ageing.</p>
<p>The post <a href="https://www.laboratorynotes.com/hutchinson-gilford-progeria-syndrome/">Hutchinson–Gilford Progeria Syndrome</a> appeared first on <a href="https://www.laboratorynotes.com">Laboratory Notes</a>.</p>
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