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	<title>Glycogen storage diseases &#8211; BIOENGINEER.ORG</title>
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		<title>Comparing Growth Impairment in Glycogen Storage Diseases</title>
		<link>https://bioengineer.org/comparing-growth-impairment-in-glycogen-storage-diseases/</link>
		
		<dc:creator><![CDATA[Bioengineer]]></dc:creator>
		<pubDate>Wed, 08 Oct 2025 02:59:13 +0000</pubDate>
				<category><![CDATA[Health]]></category>
		<category><![CDATA[enzyme deficiencies in glycogen metabolism]]></category>
		<category><![CDATA[Glycogen storage diseases]]></category>
		<category><![CDATA[growth impairment comparison]]></category>
		<category><![CDATA[GSD-I vs GSD-III/VI/IX]]></category>
		<category><![CDATA[pediatric metabolic disorders]]></category>
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					<description><![CDATA[Glycogen storage diseases (GSDs) are a group of inherited metabolic disorders that result from deficiencies in specific enzymes involved in the metabolism of glycogen. Among these conditions, Glycogen Storage Disease Type I (GSD-I) and other variants such as Types III, VI, and IX have distinct clinical manifestations and complications. A new study published in BMC [&#8230;]]]></description>
		
		
		
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