http://120.24.161.253:5617/index.php?action=history&feed=atom&title=%E9%81%97%E4%BC%A0%E6%80%A7%E7%97%89%E6%8C%9B%E6%80%A7%E6%88%AA%E7%98%AB-%E5%90%8C%E4%B9%89%E8%AF%8D-SPG 2026-06-03T00:37:17Z 本wiki的该页面的版本历史 MediaWiki 1.30.0 http://120.24.161.253:5617/index.php?title=%E9%81%97%E4%BC%A0%E6%80%A7%E7%97%89%E6%8C%9B%E6%80%A7%E6%88%AA%E7%98%AB-%E5%90%8C%E4%B9%89%E8%AF%8D-SPG&diff=2027602&oldid=prev 2026-04-16T04:37:42Z

<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=%E9%81%97%E4%BC%A0%E6%80%A7%E7%97%89%E6%8C%9B%E6%80%A7%E6%88%AA%E7%98%AB-%E5%90%8C%E4%B9%89%E8%AF%8D-SPG&diff=1992186&oldid=prev 2026-04-15T13:06:54Z

<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15日 (三) 13:06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=%E9%81%97%E4%BC%A0%E6%80%A7%E7%97%89%E6%8C%9B%E6%80%A7%E6%88%AA%E7%98%AB-%E5%90%8C%E4%B9%89%E8%AF%8D-SPG&diff=1991426&oldid=prev 2026-04-15T13:06:18Z

<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) 13:06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">遗传性痉挛截瘫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">常染色体显性遗传性痉挛性截瘫的分子遗传学进展</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>[[遗传性痉挛性截瘫]](HSP或[[SPG]])<del class="diffchange diffchange-inline">是一组具有高度临床和遗传异质性的罕见的神经系统变性疾病</del>,<del class="diffchange diffchange-inline">其发病机制复杂</del>,<del class="diffchange diffchange-inline">临床多表现为缓慢进展的双下肢无力及痉挛性截瘫</del>[<del class="diffchange diffchange-inline">1</del>]<del class="diffchange diffchange-inline">.随着病程的进展最终丧失劳动能力</del>,<del class="diffchange diffchange-inline">目前尚无有效的方法预防或延缓该种疾病的发生及进展</del>.<del class="diffchange diffchange-inline">该病发病率低</del>,<del class="diffchange diffchange-inline">基因检测作为诊断的金标准</del>.<del class="diffchange diffchange-inline">我们报道1例单纯型</del>[[遗传性痉挛性截瘫]]<del class="diffchange diffchange-inline">病例</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>[[遗传性痉挛性截瘫]](<ins class="diffchange diffchange-inline">[[SPG]])是一组以双下肢进行性肌张力增高和无力、剪刀步态为特征的具有明显临床和遗传异质性的神经系统变性疾病,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">===遗传性痉挛性截瘫患者MJD1基因的突变分析===</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 探讨中国汉族人群中[[遗传性痉挛性截瘫]](Hereditary Spastic Paraplegia,</ins>HSP或[[SPG]])<ins class="diffchange diffchange-inline">患者的MJD1基因突变特点</ins>,<ins class="diffchange diffchange-inline">进一步探索HSP和遗传性脊髓小脑性共济失调(Spinocerebellar Ataxia</ins>,<ins class="diffchange diffchange-inline">SCA)的遗传和临床</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">===不完全外显的遗传性痉挛性截瘫一家系临床与致病基因排除定位分析===</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 描述一个遗传了4代的不完全外显的</ins>[<ins class="diffchange diffchange-inline">[遗传性痉挛性截瘫]</ins>]<ins class="diffchange diffchange-inline">(hereditary spastic paraplegia,[[SPG]])大家系的临床特征</ins>,<ins class="diffchange diffchange-inline">并进行致病基因排除定位分析</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">===遗传性痉挛性截瘫一家系的临床特点与spastin基因突变分析===</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">目的探讨常染色体显性遗传的[[遗传性痉挛性截瘫]]([[SPG]])一家系的临床特点</ins>,<ins class="diffchange diffchange-inline">并行spastin基因突变分析</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">===遗传性痉挛性截瘫一家系临床及spastin基因突变的特点===</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</ins>[[遗传性痉挛性截瘫]]<ins class="diffchange diffchange-inline">([[SPG]])一家系临床及基因突变的特点</ins>.</div></td></tr> <!-- diff cache key mediawiki:diff:version:1.11a:oldid:2027601:newid:1991426 --> </table>

KGadmin http://120.24.161.253:5617/index.php?title=%E9%81%97%E4%BC%A0%E6%80%A7%E7%97%89%E6%8C%9B%E6%80%A7%E6%88%AA%E7%98%AB-%E5%90%8C%E4%B9%89%E8%AF%8D-SPG&diff=2027601&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">常染色体显性遗传性痉挛性截瘫的分子遗传学进展</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">遗传性痉挛截瘫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>[[遗传性痉挛性截瘫]](<del class="diffchange diffchange-inline">[[SPG]])是一组以双下肢进行性肌张力增高和无力、剪刀步态为特征的具有明显临床和遗传异质性的神经系统变性疾病,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.</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>[[遗传性痉挛性截瘫]](HSP或[[SPG]])<ins class="diffchange diffchange-inline">是一组具有高度临床和遗传异质性的罕见的神经系统变性疾病</ins>,<ins class="diffchange diffchange-inline">其发病机制复杂</ins>,<ins class="diffchange diffchange-inline">临床多表现为缓慢进展的双下肢无力及痉挛性截瘫</ins>[<ins class="diffchange diffchange-inline">1</ins>]<ins class="diffchange diffchange-inline">.随着病程的进展最终丧失劳动能力</ins>,<ins class="diffchange diffchange-inline">目前尚无有效的方法预防或延缓该种疾病的发生及进展</ins>.<ins class="diffchange diffchange-inline">该病发病率低</ins>,<ins class="diffchange diffchange-inline">基因检测作为诊断的金标准</ins>.<ins class="diffchange diffchange-inline">我们报道1例单纯型</ins>[[遗传性痉挛性截瘫]]<ins class="diffchange diffchange-inline">病例</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>&#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">===遗传性痉挛性截瘫患者MJD1基因的突变分析===</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 探讨中国汉族人群中[[遗传性痉挛性截瘫]](Hereditary Spastic Paraplegia,</del>HSP或[[SPG]])<del class="diffchange diffchange-inline">患者的MJD1基因突变特点</del>,<del class="diffchange diffchange-inline">进一步探索HSP和遗传性脊髓小脑性共济失调(Spinocerebellar Ataxia</del>,<del class="diffchange diffchange-inline">SCA)的遗传和临床</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>&#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">===不完全外显的遗传性痉挛性截瘫一家系临床与致病基因排除定位分析===</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 描述一个遗传了4代的不完全外显的</del>[<del class="diffchange diffchange-inline">[遗传性痉挛性截瘫</del>]<del class="diffchange diffchange-inline">](hereditary spastic paraplegia</del>,<del class="diffchange diffchange-inline">[[SPG]])大家系的临床特征,并进行致病基因排除定位分析</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>&#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">===遗传性痉挛性截瘫一家系的临床特点与spastin基因突变分析===</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">目的探讨常染色体显性遗传的[[遗传性痉挛性截瘫]]([[SPG]])一家系的临床特点</del>,<del class="diffchange diffchange-inline">并行spastin基因突变分析</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>&#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">===遗传性痉挛性截瘫一家系临床及spastin基因突变的特点===</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</del>[[遗传性痉挛性截瘫]]<del class="diffchange diffchange-inline">([[SPG]])一家系临床及基因突变的特点</del>.</div></td><td colspan="2">&#160;</td></tr> </table>

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<p>修改1</p> <p><b>新页面</b></p><div>主实体：[[遗传性痉挛性截瘫]]，关系：[[同义词]] ，尾实体：[[SPG]]<br /> <br /> ==关系介绍==<br /> 待补充<br /> <br /> ==来源==<br /> ===常染色体显性遗传性痉挛性截瘫的分子遗传学进展===<br /> [[遗传性痉挛性截瘫]]([[SPG]])是一组以双下肢进行性肌张力增高和无力、剪刀步态为特征的具有明显临床和遗传异质性的神经系统变性疾病,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.<br /> <br /> ===遗传性痉挛性截瘫患者MJD1基因的突变分析===<br /> 目的 探讨中国汉族人群中[[遗传性痉挛性截瘫]](Hereditary Spastic Paraplegia,HSP或[[SPG]])患者的MJD1基因突变特点,进一步探索HSP和遗传性脊髓小脑性共济失调(Spinocerebellar Ataxia,SCA)的遗传和临床<br /> <br /> ===不完全外显的遗传性痉挛性截瘫一家系临床与致病基因排除定位分析===<br /> 目的 描述一个遗传了4代的不完全外显的[[遗传性痉挛性截瘫]](hereditary spastic paraplegia,[[SPG]])大家系的临床特征,并进行致病基因排除定位分析.<br /> <br /> ===遗传性痉挛性截瘫一家系的临床特点与spastin基因突变分析===<br /> 目的探讨常染色体显性遗传的[[遗传性痉挛性截瘫]]([[SPG]])一家系的临床特点,并行spastin基因突变分析.<br /> <br /> ===遗传性痉挛性截瘫一家系临床及spastin基因突变的特点===<br /> 目的 探讨[[遗传性痉挛性截瘫]]([[SPG]])一家系临床及基因突变的特点.</div>

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