http://120.24.161.253:5617/index.php?action=history&feed=atom&title=%E5%85%A8%E7%BE%A7%E5%8C%96%E9%85%B6%E5%90%88%E6%88%90%E9%85%B6%E7%BC%BA%E4%B9%8F%E7%97%87-%E5%90%8C%E4%B9%89%E8%AF%8D-HCSD 2026-04-25T22:52:19Z 本wiki的该页面的版本历史 MediaWiki 1.30.0 http://120.24.161.253:5617/index.php?title=%E5%85%A8%E7%BE%A7%E5%8C%96%E9%85%B6%E5%90%88%E6%88%90%E9%85%B6%E7%BC%BA%E4%B9%8F%E7%97%87-%E5%90%8C%E4%B9%89%E8%AF%8D-HCSD&diff=2028286&oldid=prev 2026-04-16T04:38:02Z

<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) 04:38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=%E5%85%A8%E7%BE%A7%E5%8C%96%E9%85%B6%E5%90%88%E6%88%90%E9%85%B6%E7%BC%BA%E4%B9%8F%E7%97%87-%E5%90%8C%E4%B9%89%E8%AF%8D-HCSD&diff=2006666&oldid=prev 2026-04-15T13:16:53Z

<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) 13:16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; 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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">HLCS基因突变致全羧化酶合成酶缺乏症一例的临床和遗传学特点</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>[[全羧化酶合成酶缺乏症]]<del class="diffchange diffchange-inline">（holocarboxylase synthetase deficiency，</del>[[HCSD]]<del class="diffchange diffchange-inline">）是一种少见的常染色体隐性遗传病，临床表现缺乏特异性，若不及时治疗，致死率、致残率均较高。</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 探讨1例</ins>[[全羧化酶合成酶缺乏症]]<ins class="diffchange diffchange-inline">(</ins>[[HCSD]]<ins class="diffchange diffchange-inline">)患儿的临床和遗传学特点.</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">===全羧化酶合成酶缺乏症临床特点和基因突变分析===</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[[全羧化酶合成酶缺乏症]]([[HCSD]])的临床及基因突变特点.</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">===HLCS基因突变致全羧化酶合成酶缺乏症一例的临床和遗传学特点===</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1例[[全羧化酶合成酶缺乏症]]([[HCSD]])患儿的临床和遗传学特点.</ins></div></td></tr> </table>

KGadmin http://120.24.161.253:5617/index.php?title=%E5%85%A8%E7%BE%A7%E5%8C%96%E9%85%B6%E5%90%88%E6%88%90%E9%85%B6%E7%BC%BA%E4%B9%8F%E7%97%87-%E5%90%8C%E4%B9%89%E8%AF%8D-HCSD&diff=2028285&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">HLCS基因突变致全羧化酶合成酶缺乏症一例的临床和遗传学特点</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">新生儿全羧化酶合成酶缺乏症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; white-space: pre-wrap;"><div><del class="diffchange diffchange-inline">目的 探讨1例</del>[[全羧化酶合成酶缺乏症]]<del class="diffchange diffchange-inline">(</del>[[HCSD]]<del class="diffchange diffchange-inline">)患儿的临床和遗传学特点.</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>[[全羧化酶合成酶缺乏症]]<ins class="diffchange diffchange-inline">（holocarboxylase synthetase deficiency，</ins>[[HCSD]]<ins class="diffchange diffchange-inline">）是一种少见的常染色体隐性遗传病，临床表现缺乏特异性，若不及时治疗，致死率、致残率均较高。</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">===全羧化酶合成酶缺乏症临床特点和基因突变分析===</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[[全羧化酶合成酶缺乏症]]([[HCSD]])的临床及基因突变特点.</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">===HLCS基因突变致全羧化酶合成酶缺乏症一例的临床和遗传学特点===</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1例[[全羧化酶合成酶缺乏症]]([[HCSD]])患儿的临床和遗传学特点.</del></div></td><td colspan="2">&#160;</td></tr> </table>

Admin http://120.24.161.253:5617/index.php?title=%E5%85%A8%E7%BE%A7%E5%8C%96%E9%85%B6%E5%90%88%E6%88%90%E9%85%B6%E7%BC%BA%E4%B9%8F%E7%97%87-%E5%90%8C%E4%B9%89%E8%AF%8D-HCSD&diff=2006665&oldid=prev 2026-04-13T13:56:59Z

<p>修改1</p> <p><b>新页面</b></p><div>主实体：[[全羧化酶合成酶缺乏症]]，关系：[[同义词]] ，尾实体：[[HCSD]]<br /> <br /> ==关系介绍==<br /> 待补充<br /> <br /> ==来源==<br /> ===HLCS基因突变致全羧化酶合成酶缺乏症一例的临床和遗传学特点===<br /> 目的 探讨1例[[全羧化酶合成酶缺乏症]]([[HCSD]])患儿的临床和遗传学特点.<br /> <br /> ===全羧化酶合成酶缺乏症临床特点和基因突变分析===<br /> [目的]探讨[[全羧化酶合成酶缺乏症]]([[HCSD]])的临床及基因突变特点.<br /> <br /> ===HLCS基因突变致全羧化酶合成酶缺乏症一例的临床和遗传学特点===<br /> 目的 探讨1例[[全羧化酶合成酶缺乏症]]([[HCSD]])患儿的临床和遗传学特点.</div>

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