http://120.24.161.253:5617/index.php?action=history&feed=atom&title=%E8%85%93%E9%AA%A8%E8%82%8C%E8%90%8E%E7%BC%A9%E7%97%87-%E5%90%8C%E4%B9%89%E8%AF%8D-CMT 腓骨肌萎缩症-同义词-CMT - 版本历史 2026-05-09T09:48:09Z 本wiki的该页面的版本历史 MediaWiki 1.30.0 http://120.24.161.253:5617/index.php?title=%E8%85%93%E9%AA%A8%E8%82%8C%E8%90%8E%E7%BC%A9%E7%97%87-%E5%90%8C%E4%B9%89%E8%AF%8D-CMT&diff=2026706&oldid=prev KGadmin：导入1个版本 2026-04-16T04:37:19Z <p>导入1个版本</p> <table class="diff diff-contentalign-left" data-mw="interface"> <tr style="vertical-align: top;" lang="zh-CN"> <td colspan="1" style="background-color: white; color:black; text-align: center;">←上一版本</td> <td colspan="1" style="background-color: white; color:black; text-align: center;">2026年4月16日 (四) 04:37的版本</td> </tr><tr><td colspan="2" style="text-align: center;" lang="zh-CN"><div class="mw-diff-empty">（没有差异）</div> </td></tr></table> KGadmin http://120.24.161.253:5617/index.php?title=%E8%85%93%E9%AA%A8%E8%82%8C%E8%90%8E%E7%BC%A9%E7%97%87-%E5%90%8C%E4%B9%89%E8%AF%8D-CMT&diff=1990312&oldid=prev KGadmin：导入1个版本 2026-04-15T13:05:44Z <p>导入1个版本</p> <table class="diff diff-contentalign-left" data-mw="interface"> <col class="diff-marker" /> <col class="diff-content" /> <col class="diff-marker" /> <col class="diff-content" /> <tr style="vertical-align: top;" lang="zh-CN"> <td colspan="2" style="background-color: white; color:black; text-align: center;">←上一版本</td> <td colspan="2" style="background-color: white; color:black; text-align: center;">2026年4月15日 (三) 13:05的版本</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l5" >第5行：</td> <td colspan="2" class="diff-lineno">第5行：</td></tr> <tr><td class='diff-marker'>&#160;</td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'>&#160;</td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td></tr> <tr><td class='diff-marker'>&#160;</td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; 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font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div><del class="diffchange diffchange-inline">摘要 </del>[[腓骨肌萎缩症]]( [[CMT]] )<del class="diffchange diffchange-inline">是周围神经病变引起的遗传病, </del>[[CMT]]<del class="diffchange diffchange-inline">1型是最常见的亚型</del>,<del class="diffchange diffchange-inline">约占所有病例的70％</del>,<del class="diffchange diffchange-inline">常在20 岁之前发病</del>[<del class="diffchange diffchange-inline">1</del>].<del class="diffchange diffchange-inline">症状轻微者可仅有感觉不适甚至无症状,而严重者可导致瘫痪或残疾.目前已有超过100个基因被确定与</del>[[CMT]]<del class="diffchange diffchange-inline">及其相关疾病的病因相关</del>[<del class="diffchange diffchange-inline">2</del>]<del class="diffchange diffchange-inline">.基因检测已成为对该病早期诊断的重要工具.现报告1 例由PMP22 基因1 至5 号外显子单倍重复导致的</del>[[CMT]]<del class="diffchange diffchange-inline">患儿的临床资料如下</del>.</div></td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins class="diffchange diffchange-inline">目的 应用分子生物学方法对</ins>[[腓骨肌萎缩症]]([[CMT]])<ins class="diffchange diffchange-inline">患者进行外周髓鞘蛋白(PMP22)基因重复异常的检测.</ins></div></td></tr> <tr><td colspan="2">&#160;</td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>&#160;</div></td></tr> <tr><td colspan="2">&#160;</td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins class="diffchange diffchange-inline">===确诊为PMP22大片段重复突变腓骨肌萎缩症患者的临床特点===</ins></div></td></tr> <tr><td colspan="2">&#160;</td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins class="diffchange diffchange-inline">目的 探讨确诊为PMP22大片段重复突变[[腓骨肌萎缩症]]([[CMT]])患者的临床特点.</ins></div></td></tr> <tr><td colspan="2">&#160;</td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>&#160;</div></td></tr> <tr><td colspan="2">&#160;</td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins class="diffchange diffchange-inline">===慢性炎性脱髓鞘性周围神经病样表现的腓骨肌萎缩症二例===</ins></div></td></tr> <tr><td colspan="2">&#160;</td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins class="diffchange diffchange-inline">目的观察亚急性病程的慢性炎性脱髓鞘性周围神经病(CIDP)样表现的[[腓骨肌萎缩症]]([[CMT]])的临床、病理和电生理特点.</ins></div></td></tr> <tr><td colspan="2">&#160;</td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>&#160;</div></td></tr> <tr><td colspan="2">&#160;</td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins class="diffchange diffchange-inline">===X-连锁遗传性腓骨肌萎缩症的研究进展===</ins></div></td></tr> <tr><td colspan="2">&#160;</td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins class="diffchange diffchange-inline">[[腓骨肌萎缩症]](</ins>[[CMT]]<ins class="diffchange diffchange-inline">)是一组具有高度遗传异质性的周围神经系统单基因遗传病</ins>,<ins class="diffchange diffchange-inline">多数呈常染色体显性遗传</ins>,<ins class="diffchange diffchange-inline">X-连锁遗传性</ins>[<ins class="diffchange diffchange-inline">[腓骨肌萎缩症]</ins>]<ins class="diffchange diffchange-inline">([[CMT]]X)是第二常见类型</ins>.</div></td></tr> <tr><td colspan="2">&#160;</td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>&#160;</div></td></tr> <tr><td colspan="2">&#160;</td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins class="diffchange diffchange-inline">===常染色体显性遗传腓骨肌萎缩症的分子遗传学进展===</ins></div></td></tr> <tr><td colspan="2">&#160;</td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins class="diffchange diffchange-inline">[[腓骨肌萎缩症]](</ins>[[CMT]]<ins class="diffchange diffchange-inline">)亦称遗传性运动感觉神经病,是最常见的遗传性周围神经病之一,多数呈常染色体显性遗传,也可呈常染色体隐性或X连锁遗传.</ins></div></td></tr> <tr><td colspan="2">&#160;</td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>&#160;</div></td></tr> <tr><td colspan="2">&#160;</td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins class="diffchange diffchange-inline">===腓骨肌萎缩症的临床、电生理和遗传学特点(附1家系报告)===</ins></div></td></tr> <tr><td colspan="2">&#160;</td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins class="diffchange diffchange-inline">目的 探讨[</ins>[<ins class="diffchange diffchange-inline">腓骨肌萎缩症]</ins>]<ins class="diffchange diffchange-inline">(</ins>[[CMT]]<ins class="diffchange diffchange-inline">)的临床、电生理和遗传学特点</ins>.</div></td></tr> </table> KGadmin http://120.24.161.253:5617/index.php?title=%E8%85%93%E9%AA%A8%E8%82%8C%E8%90%8E%E7%BC%A9%E7%97%87-%E5%90%8C%E4%B9%89%E8%AF%8D-CMT&diff=2026705&oldid=prev Admin：修改1 2026-04-13T13:56:59Z <p>修改1</p> <table class="diff diff-contentalign-left" data-mw="interface"> <col class="diff-marker" /> <col class="diff-content" /> <col class="diff-marker" /> <col class="diff-content" /> <tr style="vertical-align: top;" lang="zh-CN"> <td colspan="2" style="background-color: white; color:black; text-align: center;">←上一版本</td> <td colspan="2" style="background-color: white; color:black; text-align: center;">2026年4月13日 (一) 13:56的版本</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l5" >第5行：</td> <td colspan="2" class="diff-lineno">第5行：</td></tr> <tr><td class='diff-marker'>&#160;</td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'>&#160;</td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td></tr> <tr><td class='diff-marker'>&#160;</td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>==来源==</div></td><td class='diff-marker'>&#160;</td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>==来源==</div></td></tr> <tr><td class='diff-marker'>−</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>===<del class="diffchange diffchange-inline">腓骨肌萎缩症基因重复异常的检测</del>===</div></td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>===<ins class="diffchange diffchange-inline">PMP22基因重复突变导致的腓骨肌萎缩症1例</ins>===</div></td></tr> <tr><td class='diff-marker'>−</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; 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font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>&#160;</div></td><td colspan="2">&#160;</td></tr> <tr><td class='diff-marker'>−</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div><del class="diffchange diffchange-inline">===确诊为PMP22大片段重复突变腓骨肌萎缩症患者的临床特点===</del></div></td><td colspan="2">&#160;</td></tr> <tr><td class='diff-marker'>−</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div><del class="diffchange diffchange-inline">目的 探讨确诊为PMP22大片段重复突变</del>[[<del class="diffchange diffchange-inline">腓骨肌萎缩症</del>]]<del class="diffchange diffchange-inline">(</del>[<del class="diffchange diffchange-inline">[CMT</del>]<del class="diffchange diffchange-inline">])患者的临床特点</del>.</div></td><td colspan="2">&#160;</td></tr> <tr><td class='diff-marker'>−</td><td style="color:black; 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font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>&#160;</div></td><td colspan="2">&#160;</td></tr> <tr><td class='diff-marker'>−</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div><del class="diffchange diffchange-inline">===腓骨肌萎缩症的临床、电生理和遗传学特点(附1家系报告)===</del></div></td><td colspan="2">&#160;</td></tr> <tr><td class='diff-marker'>−</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div><del class="diffchange diffchange-inline">目的 探讨[[腓骨肌萎缩症]](</del>[[CMT]]<del class="diffchange diffchange-inline">)的临床、电生理和遗传学特点</del>.</div></td><td colspan="2">&#160;</td></tr> </table> Admin http://120.24.161.253:5617/index.php?title=%E8%85%93%E9%AA%A8%E8%82%8C%E8%90%8E%E7%BC%A9%E7%97%87-%E5%90%8C%E4%B9%89%E8%AF%8D-CMT&diff=1990311&oldid=prev Admin：修改1 2026-04-13T13:56:59Z <p>修改1</p> <table class="diff diff-contentalign-left" data-mw="interface"> <col class="diff-marker" /> <col class="diff-content" /> <col class="diff-marker" /> <col class="diff-content" /> <tr style="vertical-align: top;" lang="zh-CN"> <td colspan="2" style="background-color: white; color:black; text-align: center;">←上一版本</td> <td colspan="2" style="background-color: white; color:black; text-align: center;">2026年4月13日 (一) 13:56的版本</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l1" >第1行：</td> <td colspan="2" class="diff-lineno">第1行：</td></tr> <tr><td class='diff-marker'>&#160;</td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>主实体：[[腓骨肌萎缩症]]，关系：[[同义词]] ，尾实体：[[CMT]]</div></td><td class='diff-marker'>&#160;</td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>主实体：[[腓骨肌萎缩症]]，关系：[[同义词]] ，尾实体：[[CMT]]</div></td></tr> <tr><td class='diff-marker'>&#160;</td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'>&#160;</td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td></tr> <tr><td class='diff-marker'>−</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div><del style="font-weight: bold; text-decoration: none;">实体ID:''301052''</del></div></td><td colspan="2">&#160;</td></tr> <tr><td class='diff-marker'>&#160;</td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>==关系介绍==</div></td><td class='diff-marker'>&#160;</td><td style="background-color: #f9f9f9; 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border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'>&#160;</td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td></tr> <tr><td class='diff-marker'>−</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>===<del class="diffchange diffchange-inline">确诊为PMP22大片段重复突变腓骨肌萎缩症患者的临床特点（中华医学会文献）</del>===</div></td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>===<ins class="diffchange diffchange-inline">确诊为PMP22大片段重复突变腓骨肌萎缩症患者的临床特点</ins>===</div></td></tr> <tr><td class='diff-marker'>&#160;</td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>目的 探讨确诊为PMP22大片段重复突变[[腓骨肌萎缩症]]([[CMT]])患者的临床特点.</div></td><td class='diff-marker'>&#160;</td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>目的 探讨确诊为PMP22大片段重复突变[[腓骨肌萎缩症]]([[CMT]])患者的临床特点.</div></td></tr> <tr><td class='diff-marker'>&#160;</td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'>&#160;</td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td></tr> <tr><td class='diff-marker'>−</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>===<del class="diffchange diffchange-inline">慢性炎性脱髓鞘性周围神经病样表现的腓骨肌萎缩症二例（中华医学会文献）</del>===</div></td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>===<ins class="diffchange diffchange-inline">慢性炎性脱髓鞘性周围神经病样表现的腓骨肌萎缩症二例</ins>===</div></td></tr> <tr><td class='diff-marker'>&#160;</td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>目的观察亚急性病程的慢性炎性脱髓鞘性周围神经病(CIDP)样表现的[[腓骨肌萎缩症]]([[CMT]])的临床、病理和电生理特点.</div></td><td class='diff-marker'>&#160;</td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>目的观察亚急性病程的慢性炎性脱髓鞘性周围神经病(CIDP)样表现的[[腓骨肌萎缩症]]([[CMT]])的临床、病理和电生理特点.</div></td></tr> <tr><td class='diff-marker'>&#160;</td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'>&#160;</td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td></tr> <tr><td class='diff-marker'>−</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>===X-<del class="diffchange diffchange-inline">连锁遗传性腓骨肌萎缩症的研究进展（中华医学会文献）</del>===</div></td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>===X-<ins class="diffchange diffchange-inline">连锁遗传性腓骨肌萎缩症的研究进展</ins>===</div></td></tr> <tr><td class='diff-marker'>&#160;</td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>[[腓骨肌萎缩症]]([[CMT]])是一组具有高度遗传异质性的周围神经系统单基因遗传病,多数呈常染色体显性遗传,X-连锁遗传性[[腓骨肌萎缩症]]([[CMT]]X)是第二常见类型.</div></td><td class='diff-marker'>&#160;</td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>[[腓骨肌萎缩症]]([[CMT]])是一组具有高度遗传异质性的周围神经系统单基因遗传病,多数呈常染色体显性遗传,X-连锁遗传性[[腓骨肌萎缩症]]([[CMT]]X)是第二常见类型.</div></td></tr> <tr><td class='diff-marker'>&#160;</td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'>&#160;</td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"></td></tr> <tr><td class='diff-marker'>−</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>===<del class="diffchange diffchange-inline">常染色体显性遗传腓骨肌萎缩症的分子遗传学进展（中华医学会文献）</del>===</div></td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>===<ins class="diffchange diffchange-inline">常染色体显性遗传腓骨肌萎缩症的分子遗传学进展</ins>===</div></td></tr> <tr><td class='diff-marker'>&#160;</td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>[[腓骨肌萎缩症]]([[CMT]])亦称遗传性运动感觉神经病,是最常见的遗传性周围神经病之一,多数呈常染色体显性遗传,也可呈常染色体隐性或X连锁遗传.</div></td><td class='diff-marker'>&#160;</td><td style="background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;"><div>[[腓骨肌萎缩症]]([[CMT]])亦称遗传性运动感觉神经病,是最常见的遗传性周围神经病之一,多数呈常染色体显性遗传,也可呈常染色体隐性或X连锁遗传.</div></td></tr> <tr><td colspan="2">&#160;</td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;"></ins></div></td></tr> <tr><td colspan="2">&#160;</td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">===腓骨肌萎缩症的临床、电生理和遗传学特点(附1家系报告)===</ins></div></td></tr> <tr><td colspan="2">&#160;</td><td class='diff-marker'>+</td><td style="color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">目的 探讨[[腓骨肌萎缩症]]([[CMT]])的临床、电生理和遗传学特点.</ins></div></td></tr> </table> Admin http://120.24.161.253:5617/index.php?title=%E8%85%93%E9%AA%A8%E8%82%8C%E8%90%8E%E7%BC%A9%E7%97%87-%E5%90%8C%E4%B9%89%E8%AF%8D-CMT&diff=1794740&oldid=prev Admin：修改1 2024-07-06T14:00:00Z <p>修改1</p> <table class="diff diff-contentalign-left" data-mw="interface"> <tr style="vertical-align: top;" lang="zh-CN"> <td colspan="1" style="background-color: white; color:black; text-align: center;">←上一版本</td> <td colspan="1" style="background-color: white; color:black; text-align: center;">2024年7月6日 (六) 14:00的版本</td> </tr><tr><td colspan="2" style="text-align: center;" lang="zh-CN"><div class="mw-diff-empty">（没有差异）</div> </td></tr></table> Admin http://120.24.161.253:5617/index.php?title=%E8%85%93%E9%AA%A8%E8%82%8C%E8%90%8E%E7%BC%A9%E7%97%87-%E5%90%8C%E4%B9%89%E8%AF%8D-CMT&diff=1794741&oldid=prev KGadmin：导入1个版本 2024-07-06T13:11:13Z <p>导入1个版本</p> <table class="diff diff-contentalign-left" data-mw="interface"> <tr style="vertical-align: top;" lang="zh-CN"> <td colspan="1" style="background-color: white; color:black; text-align: center;">←上一版本</td> <td colspan="1" style="background-color: white; color:black; text-align: center;">2024年7月6日 (六) 13:11的版本</td> </tr><tr><td colspan="2" style="text-align: center;" lang="zh-CN"><div class="mw-diff-empty">（没有差异）</div> </td></tr></table> KGadmin http://120.24.161.253:5617/index.php?title=%E8%85%93%E9%AA%A8%E8%82%8C%E8%90%8E%E7%BC%A9%E7%97%87-%E5%90%8C%E4%B9%89%E8%AF%8D-CMT&diff=194384&oldid=prev Admin：导入1个版本 2021-10-21T07:55:27Z <p>导入1个版本</p> <table class="diff diff-contentalign-left" data-mw="interface"> <tr style="vertical-align: top;" lang="zh-CN"> <td colspan="1" style="background-color: white; color:black; text-align: center;">←上一版本</td> <td colspan="1" style="background-color: white; color:black; text-align: center;">2021年10月21日 (四) 07:55的版本</td> </tr><tr><td colspan="2" style="text-align: center;" lang="zh-CN"><div class="mw-diff-empty">（没有差异）</div> </td></tr></table> Admin http://120.24.161.253:5617/index.php?title=%E8%85%93%E9%AA%A8%E8%82%8C%E8%90%8E%E7%BC%A9%E7%97%87-%E5%90%8C%E4%B9%89%E8%AF%8D-CMT&diff=194375&oldid=prev Admin：修改1 2021-10-19T13:56:59Z <p>修改1</p> <p><b>新页面</b></p><div>主实体：[[腓骨肌萎缩症]]，关系：[[同义词]] ，尾实体：[[CMT]]<br /> <br /> 实体ID:''301052''<br /> ==关系介绍==<br /> 待补充<br /> <br /> ==来源==<br /> ===腓骨肌萎缩症基因重复异常的检测（中华医学会文献）===<br /> 目的 应用分子生物学方法对[[腓骨肌萎缩症]]([[CMT]])患者进行外周髓鞘蛋白(PMP22)基因重复异常的检测.<br /> <br /> ===确诊为PMP22大片段重复突变腓骨肌萎缩症患者的临床特点（中华医学会文献）===<br /> 目的 探讨确诊为PMP22大片段重复突变[[腓骨肌萎缩症]]([[CMT]])患者的临床特点.<br /> <br /> ===慢性炎性脱髓鞘性周围神经病样表现的腓骨肌萎缩症二例（中华医学会文献）===<br /> 目的观察亚急性病程的慢性炎性脱髓鞘性周围神经病(CIDP)样表现的[[腓骨肌萎缩症]]([[CMT]])的临床、病理和电生理特点.<br /> <br /> ===X-连锁遗传性腓骨肌萎缩症的研究进展（中华医学会文献）===<br /> [[腓骨肌萎缩症]]([[CMT]])是一组具有高度遗传异质性的周围神经系统单基因遗传病,多数呈常染色体显性遗传,X-连锁遗传性[[腓骨肌萎缩症]]([[CMT]]X)是第二常见类型.<br /> <br /> ===常染色体显性遗传腓骨肌萎缩症的分子遗传学进展（中华医学会文献）===<br /> [[腓骨肌萎缩症]]([[CMT]])亦称遗传性运动感觉神经病,是最常见的遗传性周围神经病之一,多数呈常染色体显性遗传,也可呈常染色体隐性或X连锁遗传.</div> Admin