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	<title>SLC20A2 Mutations &#8211; BIOENGINEER.ORG</title>
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	<title>SLC20A2 Mutations &#8211; BIOENGINEER.ORG</title>
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		<title>First Libyan Children with SLC20A2 Mutations and Fahr’s Disease</title>
		<link>https://bioengineer.org/first-libyan-children-with-slc20a2-mutations-and-fahrs-disease/</link>
		
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		<pubDate>Sat, 24 Jan 2026 15:09:44 +0000</pubDate>
				<category><![CDATA[Health]]></category>
		<category><![CDATA[Fahr's Disease]]></category>
		<category><![CDATA[Libyan children]]></category>
		<category><![CDATA[Libyan Medical Case]]></category>
		<category><![CDATA[Pediatric Neurology]]></category>
		<category><![CDATA[rare genetic disorders]]></category>
		<category><![CDATA[SLC20A2 Mutations]]></category>
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					<description><![CDATA[In a groundbreaking study that has ramifications for pediatric neurology, a research team in Libya has revealed the first documented case of Fahr’s disease linked to homozygous mutations in the SLC20A2 gene. This fascinating discovery provides not only insights into the genetic underpinnings of this rare disorder but also highlights the importance of understanding these [&#8230;]]]></description>
		
		
		
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