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		<title>苯丙酮尿症-临床表现-智力发育不全 - 版本历史</title>
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		<updated>2026-06-04T17:47:15Z</updated>
		<subtitle>本wiki的该页面的版本历史</subtitle>
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		<title>KGadmin：导入1个版本</title>
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				<updated>2026-04-15T13:07:30Z</updated>
		
		<summary type="html">&lt;p&gt;导入1个版本&lt;/p&gt;
&lt;table class=&quot;diff diff-contentalign-left&quot; data-mw=&quot;interface&quot;&gt;
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		<author><name>KGadmin</name></author>	</entry>

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		<title>Admin：修改1</title>
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				<updated>2026-04-13T13:56:59Z</updated>
		
		<summary type="html">&lt;p&gt;修改1&lt;/p&gt;
&lt;p&gt;&lt;b&gt;新页面&lt;/b&gt;&lt;/p&gt;&lt;div&gt;主实体：[[苯丙酮尿症]]，关系：[[临床表现]] ，尾实体：[[智力发育不全]]&lt;br /&gt;
&lt;br /&gt;
==关系介绍==&lt;br /&gt;
待补充&lt;br /&gt;
&lt;br /&gt;
==来源==&lt;br /&gt;
===苯丙酮尿症的实验室诊断与防治措施===&lt;br /&gt;
[[苯丙酮尿症]]是一种因缺乏苯丙氨酸羟化酶或四氢生物蝶呤合成酶所致的苯丙氨酸代谢异常引起的隐性遗传病,患者的主要临床特征为[[智力发育不全]]、语言障碍、毛发和皮肤颜色变浅、癫痫、尿和汗液有鼠臭气味等.&lt;/div&gt;</summary>
		<author><name>Admin</name></author>	</entry>

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