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		<title>强直性肌营养不良-临床表现-肌病面容 - 版本历史</title>
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		<updated>2026-04-17T16:39:09Z</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>2026-04-15T13:17:26Z</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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				&lt;td colspan=&quot;1&quot; style=&quot;background-color: white; color:black; text-align: center;&quot;&gt;←上一版本&lt;/td&gt;
				&lt;td colspan=&quot;1&quot; style=&quot;background-color: white; color:black; text-align: center;&quot;&gt;2026年4月15日 (三) 13:17的版本&lt;/td&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：[[强直性肌营养不良]]，关系：[[临床表现]] ，尾实体：[[肌病面容]]&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;
===强直性肌营养不良（2019年版诊疗指南）===&lt;br /&gt;
[[强直性肌营养不良]]的诊断依靠病史（常染色体显性遗传家族史、“遗传早现”现象和肌强直现象）、特征性体征（远端或轴位为主肌肉无力萎缩、[[肌病面容]]、肌球现象、额秃等）、肌电图、心电图、眼科、内分泌检查发现多系统损害，最终通过基因检测确诊。&lt;/div&gt;</summary>
		<author><name>Admin</name></author>	</entry>

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