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		<id>https://teaching.ncl.ac.uk/bms/wiki//index.php?title=Von_Gierke_disease&amp;diff=22820</id>
		<title>Von Gierke disease</title>
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		<updated>2018-12-05T16:47:51Z</updated>

		<summary type="html">&lt;p&gt;180163687: Created page with &amp;quot;&amp;amp;nbsp;Von Gierke disease is also known as Type I Glycogen Storage Disease (GSD I)&amp;lt;ref&amp;gt;https://medlineplus.gov/ency/article/000338.htm [cited 05/11/18]&amp;lt;/ref&amp;gt;. It is caused by a gl...&amp;quot;&lt;/p&gt;
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&lt;div&gt;&amp;amp;nbsp;Von Gierke disease is also known as Type I Glycogen Storage Disease (GSD I)&amp;lt;ref&amp;gt;https://medlineplus.gov/ency/article/000338.htm [cited 05/11/18]&amp;lt;/ref&amp;gt;. It is caused by a glucose-6-phosphatase deficiency, and so leads to the body being unable to break down [[Glycogen|glycogen]] into [[Glucose|glucose]] during [[Glycogenolysis|glycogenolysis]] in the liver&amp;lt;ref&amp;gt;BGM1002 Lecture 28&amp;lt;/ref&amp;gt;. This leads to [[Hypoglycaemia|hypoglycaemia]] and [[Hepatomegaly|hepatomegaly]]. Von Gierke disease is inherited.&lt;br /&gt;
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		<author><name>180163687</name></author>
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