http://120.24.161.253:5617/index.php?action=history&feed=atom&title=%E8%84%8A%E9%AB%93%E5%B0%8F%E8%84%91%E6%80%A7%E5%85%B1%E6%B5%8E%E5%A4%B1%E8%B0%83-%E9%81%97%E4%BC%A0%E5%9B%A0%E7%B4%A0-%E5%B8%B8%E6%9F%93%E8%89%B2%E4%BD%93%E6%98%BE%E6%80%A7%E9%81%97%E4%BC%A0 2026-04-17T20:54:57Z 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%84%8A%E9%AB%93%E5%B0%8F%E8%84%91%E6%80%A7%E5%85%B1%E6%B5%8E%E5%A4%B1%E8%B0%83-%E9%81%97%E4%BC%A0%E5%9B%A0%E7%B4%A0-%E5%B8%B8%E6%9F%93%E8%89%B2%E4%BD%93%E6%98%BE%E6%80%A7%E9%81%97%E4%BC%A0&diff=2028072&oldid=prev 2026-04-16T04:37:46Z

<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%84%8A%E9%AB%93%E5%B0%8F%E8%84%91%E6%80%A7%E5%85%B1%E6%B5%8E%E5%A4%B1%E8%B0%83-%E9%81%97%E4%BC%A0%E5%9B%A0%E7%B4%A0-%E5%B8%B8%E6%9F%93%E8%89%B2%E4%BD%93%E6%98%BE%E6%80%A7%E9%81%97%E4%BC%A0&diff=2012060&oldid=prev 2026-04-15T13:21:20Z

<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) 13:21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">CCDC88C基因突变致脊髓小脑性共济失调40型1例</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">脊髓小脑性共济失调1例分析并文献复习</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; white-space: pre-wrap;"><div><del class="diffchange diffchange-inline">摘要 </del>[[脊髓小脑性共济失调]]<del class="diffchange diffchange-inline">(spinocerebellar ataxias,SCAs)是遗传性共济失调的主要类型,以进行性共济失调为其特征性的临床表现,还可伴有眼球运动障碍、视神经萎缩、视网膜色素变性、锥体束征、锥体外系体征、肌萎缩、周围神经病和痴呆等.该病多为</del>[[常染色体显性遗传]],<del class="diffchange diffchange-inline">已明确的致病基因达48个,具有高度基因和临床异质性,目前对不同基因型的自然史研究逐步深入,不同基因背景下疾病进展速度和主要临床表现各异[1-5]</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">结论:</ins>[[脊髓小脑性共济失调]]<ins class="diffchange diffchange-inline">是一种</ins>[[常染色体显性遗传]]<ins class="diffchange diffchange-inline">疾病</ins>,<ins class="diffchange diffchange-inline">共济失调为其主要临床表现</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;"></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">晚发型脊髓小脑性共济失调3型1例报告</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">脊髓小脑性共济失调的研究进展</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; white-space: pre-wrap;"><div><del class="diffchange diffchange-inline">摘要 </del>[[脊髓小脑性共济失调]](SCA)<del class="diffchange diffchange-inline">是具有临床和遗传异质性的神经系统疾病,多呈</del>[[常染色体显性遗传]],<del class="diffchange diffchange-inline">主要表现为慢性进行性加重的共济失调、构音障碍及眼球运动障碍等.现报道的SCA 亚型多达40 种,其发病年龄及临床症状多相互重叠[1] ,仅依据临床特征及影像学检查明确分型较为困难,基因检测有助于进一步明确诊断.本文报道1 例确诊为晚发型SCA3型(SCA3)的病例如下</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>[[脊髓小脑性共济失调]](<ins class="diffchange diffchange-inline">spinocerebellar ataxia,</ins>SCA)<ins class="diffchange diffchange-inline">是一组</ins>[[常染色体显性遗传]]<ins class="diffchange diffchange-inline">的进行性加重的神经系统退行性疾病</ins>,<ins class="diffchange diffchange-inline">核心症状为小脑共济失调</ins>.</div></td></tr> </table>

KGadmin http://120.24.161.253:5617/index.php?title=%E8%84%8A%E9%AB%93%E5%B0%8F%E8%84%91%E6%80%A7%E5%85%B1%E6%B5%8E%E5%A4%B1%E8%B0%83-%E9%81%97%E4%BC%A0%E5%9B%A0%E7%B4%A0-%E5%B8%B8%E6%9F%93%E8%89%B2%E4%BD%93%E6%98%BE%E6%80%A7%E9%81%97%E4%BC%A0&diff=2028071&oldid=prev 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">脊髓小脑性共济失调1例分析并文献复习</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">CCDC88C基因突变致脊髓小脑性共济失调40型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; white-space: pre-wrap;"><div><del class="diffchange diffchange-inline">结论:</del>[[脊髓小脑性共济失调]]<del class="diffchange diffchange-inline">是一种</del>[[常染色体显性遗传]]<del class="diffchange diffchange-inline">疾病</del>,<del class="diffchange diffchange-inline">共济失调为其主要临床表现</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">摘要 </ins>[[脊髓小脑性共济失调]]<ins class="diffchange diffchange-inline">(spinocerebellar ataxias,SCAs)是遗传性共济失调的主要类型,以进行性共济失调为其特征性的临床表现,还可伴有眼球运动障碍、视神经萎缩、视网膜色素变性、锥体束征、锥体外系体征、肌萎缩、周围神经病和痴呆等.该病多为</ins>[[常染色体显性遗传]],<ins class="diffchange diffchange-inline">已明确的致病基因达48个,具有高度基因和临床异质性,目前对不同基因型的自然史研究逐步深入,不同基因背景下疾病进展速度和主要临床表现各异[1-5]</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;"></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">脊髓小脑性共济失调的研究进展</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">晚发型脊髓小脑性共济失调3型1例报告</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; white-space: pre-wrap;"><div>[[脊髓小脑性共济失调]](<del class="diffchange diffchange-inline">spinocerebellar ataxia,</del>SCA)<del class="diffchange diffchange-inline">是一组</del>[[常染色体显性遗传]]<del class="diffchange diffchange-inline">的进行性加重的神经系统退行性疾病</del>,<del class="diffchange diffchange-inline">核心症状为小脑共济失调</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">摘要 </ins>[[脊髓小脑性共济失调]](SCA)<ins class="diffchange diffchange-inline">是具有临床和遗传异质性的神经系统疾病,多呈</ins>[[常染色体显性遗传]],<ins class="diffchange diffchange-inline">主要表现为慢性进行性加重的共济失调、构音障碍及眼球运动障碍等.现报道的SCA 亚型多达40 种,其发病年龄及临床症状多相互重叠[1] ,仅依据临床特征及影像学检查明确分型较为困难,基因检测有助于进一步明确诊断.本文报道1 例确诊为晚发型SCA3型(SCA3)的病例如下</ins>.</div></td></tr> </table>

Admin http://120.24.161.253:5617/index.php?title=%E8%84%8A%E9%AB%93%E5%B0%8F%E8%84%91%E6%80%A7%E5%85%B1%E6%B5%8E%E5%A4%B1%E8%B0%83-%E9%81%97%E4%BC%A0%E5%9B%A0%E7%B4%A0-%E5%B8%B8%E6%9F%93%E8%89%B2%E4%BD%93%E6%98%BE%E6%80%A7%E9%81%97%E4%BC%A0&diff=2012059&oldid=prev 2026-04-13T13:56:59Z

<p>修改1</p> <p><b>新页面</b></p><div>主实体：[[脊髓小脑性共济失调]]，关系：[[遗传因素]] ，尾实体：[[常染色体显性遗传]]<br /> <br /> ==关系介绍==<br /> 待补充<br /> <br /> ==来源==<br /> ===脊髓小脑性共济失调1例分析并文献复习===<br /> 结论:[[脊髓小脑性共济失调]]是一种[[常染色体显性遗传]]疾病,共济失调为其主要临床表现.<br /> <br /> ===脊髓小脑性共济失调的研究进展===<br /> [[脊髓小脑性共济失调]](spinocerebellar ataxia,SCA)是一组[[常染色体显性遗传]]的进行性加重的神经系统退行性疾病,核心症状为小脑共济失调.</div>

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