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-%E5%90%8C%E4%B9%89%E8%AF%8D-spinocerebellar_ataxia 2026-05-25T09:40:55Z 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-%E5%90%8C%E4%B9%89%E8%AF%8D-spinocerebellar_ataxia&diff=2028080&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-%E5%90%8C%E4%B9%89%E8%AF%8D-spinocerebellar_ataxia&diff=2012046&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">以帕金森综合征为主要表现的脊髓小脑性共济失调3型一例</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">中国汉族人群ATXN8OS基因CTA/CTG三核苷酸重复研究</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]]([[spinocerebellar ataxia]],SCA)<del class="diffchange diffchange-inline">是一组高度遗传异质性疾病</del>,<del class="diffchange diffchange-inline">包括多种亚型</del>[<del class="diffchange diffchange-inline">1</del>],<del class="diffchange diffchange-inline">我国以SCA3最常见</del>,<del class="diffchange diffchange-inline">也称为马查多-约瑟夫病</del>(<del class="diffchange diffchange-inline">Machado-Joseph disease</del>,<del class="diffchange diffchange-inline">MJD</del>)[<del class="diffchange diffchange-inline">2</del>].<del class="diffchange diffchange-inline">SCA3的核心表现包括为突眼、小脑性共济失调、肌强直、锥体束征、肌萎缩等</del>,<del class="diffchange diffchange-inline">而以帕金森综合征为主要表现的SCA3病例较为少见.本文报道一例少见的以帕金森综合征为主要表现的SCA3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><ins class="diffchange diffchange-inline">目的 研究中国正常人群</ins>[[脊髓小脑性共济失调]]([[spinocerebellar ataxia]],SCA)<ins class="diffchange diffchange-inline">8型(SCA8)致病基因ATXN8OS(CTA/CTG)n正常变异范围</ins>,<ins class="diffchange diffchange-inline">以及AIXN8OS基因(CTA/CTG)n扩展突变在中国大陆SCA患者中的分布.</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">===安徽脊髓小脑性共济失调患者基因型与中医证型相关性===</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 通过探讨[</ins>[<ins class="diffchange diffchange-inline">脊髓小脑性共济失调]]([[spinocerebellar ataxia]</ins>],<ins class="diffchange diffchange-inline">SCA)患者基因型与中医证型的关系</ins>,<ins class="diffchange diffchange-inline">为SCA的辨证客观化提供依据.</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">===遗传性脊髓小脑共济失调3型M RI 检查的应用及进展===</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">[[脊髓小脑性共济失调]]（[[spinocerebellar ataxia]] ，SCA）是一组以迟发、进展性小脑及其传入和传出连接功能退化为特点的遗传性神经系统变性疾病，该病根据基因、染色体位点及生化产物可分为SCA 1‐SCA 29等约30种，中国发病率最高的亚型为</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">===脊髓小脑性共济失调3型一家系报道===</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[[脊髓小脑性共济失调]]</ins>(<ins class="diffchange diffchange-inline">[[spinocerebellar ataxia]]</ins>,<ins class="diffchange diffchange-inline">SCA)3型(SCA3</ins>)<ins class="diffchange diffchange-inline">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">===脊髓小脑性共济失调的研究进展===</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">[脊髓小脑性共济失调]]([[spinocerebellar ataxia]</ins>]<ins class="diffchange diffchange-inline">,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</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">===脊髓小脑共济失调患者CAG病理重复次数检测===</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><ins class="diffchange diffchange-inline">目的 研究中国汉族人群[[脊髓小脑性共济失调]]([[spinocerebellar ataxia]]</ins>,<ins class="diffchange diffchange-inline">SCA)1、2、3、6、7、12、17亚型致病基因的CAG三核苷酸病理重复次数范围</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-%E5%90%8C%E4%B9%89%E8%AF%8D-spinocerebellar_ataxia&diff=2028079&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">中国汉族人群ATXN8OS基因CTA/CTG三核苷酸重复研究</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">以帕金森综合征为主要表现的脊髓小脑性共济失调3型一例</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">目的 研究中国正常人群</del>[[脊髓小脑性共济失调]]([[spinocerebellar ataxia]],SCA)<del class="diffchange diffchange-inline">8型(SCA8)致病基因ATXN8OS(CTA/CTG)n正常变异范围</del>,<del class="diffchange diffchange-inline">以及AIXN8OS基因(CTA/CTG)n扩展突变在中国大陆SCA患者中的分布.</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]]([[spinocerebellar ataxia]],SCA)<ins class="diffchange diffchange-inline">是一组高度遗传异质性疾病</ins>,<ins class="diffchange diffchange-inline">包括多种亚型</ins>[<ins class="diffchange diffchange-inline">1</ins>],<ins class="diffchange diffchange-inline">我国以SCA3最常见</ins>,<ins class="diffchange diffchange-inline">也称为马查多-约瑟夫病</ins>(<ins class="diffchange diffchange-inline">Machado-Joseph disease</ins>,<ins class="diffchange diffchange-inline">MJD</ins>)[<ins class="diffchange diffchange-inline">2</ins>]<ins class="diffchange diffchange-inline">.SCA3的核心表现包括为突眼、小脑性共济失调、肌强直、锥体束征、肌萎缩等</ins>,<ins class="diffchange diffchange-inline">而以帕金森综合征为主要表现的SCA3病例较为少见</ins>.<ins class="diffchange diffchange-inline">本文报道一例少见的以帕金森综合征为主要表现的SCA3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">===安徽脊髓小脑性共济失调患者基因型与中医证型相关性===</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 通过探讨[</del>[<del class="diffchange diffchange-inline">脊髓小脑性共济失调]]([[spinocerebellar ataxia]</del>],<del class="diffchange diffchange-inline">SCA)患者基因型与中医证型的关系</del>,<del class="diffchange diffchange-inline">为SCA的辨证客观化提供依据.</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">===遗传性脊髓小脑共济失调3型M RI 检查的应用及进展===</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">[[脊髓小脑性共济失调]]（[[spinocerebellar ataxia]] ，SCA）是一组以迟发、进展性小脑及其传入和传出连接功能退化为特点的遗传性神经系统变性疾病，该病根据基因、染色体位点及生化产物可分为SCA 1‐SCA 29等约30种，中国发病率最高的亚型为</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">===脊髓小脑性共济失调3型一家系报道===</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[[脊髓小脑性共济失调]]</del>(<del class="diffchange diffchange-inline">[[spinocerebellar ataxia]]</del>,<del class="diffchange diffchange-inline">SCA)3型(SCA3</del>)<del class="diffchange diffchange-inline">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>&#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">===脊髓小脑性共济失调的研究进展===</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">[脊髓小脑性共济失调</del>]<del class="diffchange diffchange-inline">]([[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</del>,<del class="diffchange diffchange-inline">核心症状为小脑共济失调</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">===脊髓小脑共济失调患者CAG病理重复次数检测===</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 研究中国汉族人群[[脊髓小脑性共济失调]]([[spinocerebellar ataxia]],SCA)1、2、3、6、7、12、17亚型致病基因的CAG三核苷酸病理重复次数范围</del>.</div></td><td colspan="2">&#160;</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-%E5%90%8C%E4%B9%89%E8%AF%8D-spinocerebellar_ataxia&diff=2012045&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：[[同义词]] ，尾实体：[[spinocerebellar ataxia]]<br /> <br /> ==关系介绍==<br /> 待补充<br /> <br /> ==来源==<br /> ===中国汉族人群ATXN8OS基因CTA/CTG三核苷酸重复研究===<br /> 目的 研究中国正常人群[[脊髓小脑性共济失调]]([[spinocerebellar ataxia]],SCA)8型(SCA8)致病基因ATXN8OS(CTA/CTG)n正常变异范围,以及AIXN8OS基因(CTA/CTG)n扩展突变在中国大陆SCA患者中的分布.<br /> <br /> ===安徽脊髓小脑性共济失调患者基因型与中医证型相关性===<br /> 目的 通过探讨[[脊髓小脑性共济失调]]([[spinocerebellar ataxia]],SCA)患者基因型与中医证型的关系,为SCA的辨证客观化提供依据.<br /> <br /> ===遗传性脊髓小脑共济失调3型M RI 检查的应用及进展===<br /> [[脊髓小脑性共济失调]]（[[spinocerebellar ataxia]] ，SCA）是一组以迟发、进展性小脑及其传入和传出连接功能退化为特点的遗传性神经系统变性疾病，该病根据基因、染色体位点及生化产物可分为SCA 1‐SCA 29等约30种，中国发病率最高的亚型为<br /> <br /> ===脊髓小脑性共济失调3型一家系报道===<br /> 目的 探讨[[脊髓小脑性共济失调]]([[spinocerebellar ataxia]],SCA)3型(SCA3)的临床特点.<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.<br /> <br /> ===脊髓小脑共济失调患者CAG病理重复次数检测===<br /> 目的 研究中国汉族人群[[脊髓小脑性共济失调]]([[spinocerebellar ataxia]],SCA)1、2、3、6、7、12、17亚型致病基因的CAG三核苷酸病理重复次数范围.</div>

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