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	<title>Werner syndrome Archives - Laboratory Notes</title>
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		<title>Progeroid Syndromes</title>
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		<pubDate>Sat, 22 Aug 2026 16:44:18 +0000</pubDate>
				<category><![CDATA[Lab Notes]]></category>
		<category><![CDATA[Lab Notes: Biology]]></category>
		<category><![CDATA[Lab Notes: Cell Biology]]></category>
		<category><![CDATA[Genomic instability]]></category>
		<category><![CDATA[Hutchinson–Gilford progeria]]></category>
		<category><![CDATA[Premature ageing]]></category>
		<category><![CDATA[Progeroid syndromes]]></category>
		<category><![CDATA[Telomere dysfunction]]></category>
		<category><![CDATA[Werner syndrome]]></category>
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					<description><![CDATA[<p>Progeroid syndromes are rare genetic disorders that cause premature ageing due to defects in nuclear‑lamina structure, telomere maintenance and DNA‑repair pathways. Mutations in genes such as LMNA, WRN and TERT accelerate cellular decline, leading to early onset of ageing features and increased susceptibility to cardiovascular, metabolic and degenerative diseases.</p>
<p>The post <a href="https://www.laboratorynotes.com/progeroid-syndromes/">Progeroid Syndromes</a> appeared first on <a href="https://www.laboratorynotes.com">Laboratory Notes</a>.</p>
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