https://idwiki.org/index.php?action=history&feed=atom&title=Wiskott-Aldrich_syndrome 2026-04-28T22:15:48Z Revision history for this page on the wiki MediaWiki 1.43.8 https://idwiki.org/index.php?title=Wiskott-Aldrich_syndrome&diff=11318&oldid=prev 2025-10-06T20:20:22Z

<p></p> <table style="background-color: #fff; color: #202122;" data-mw="interface"> <col class="diff-marker" /> <col class="diff-content" /> <col class="diff-marker" /> <col class="diff-content" /> <tr class="diff-title" lang="en"> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 20:20, 6 October 2025</td> </tr><tr> <td colspan="2" class="diff-lineno">Line 1:</td> <td colspan="2" class="diff-lineno">Line 1:</td> </tr> <tr> <td class="diff-marker"></td> <td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>* [[Primary immunodeficiency]]</div></td> <td class="diff-marker"></td> <td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>* [[Primary immunodeficiency]]</div></td> </tr> <tr> <td class="diff-marker" data-marker="−"></td> <td style="color: #202122; 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-linked recessive defect in the <del style="font-weight: bold; text-decoration: none;">WAS</del> gene located at xP 11.22-23</div></td> <td class="diff-marker" data-marker="+"></td> <td style="color: #202122; 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-linked recessive defect in the <ins style="font-weight: bold; text-decoration: none;">WASp</ins> gene located at xP 11.22-23</div></td> </tr> <tr> <td class="diff-marker" data-marker="−"></td> <td style="color: #202122; 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>* Characterized by [[eczema]], [[thrombocytopenia]], [[immunodeficiency]]</div></td> <td class="diff-marker" data-marker="+"></td> <td style="color: #202122; 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>* Characterized by [[eczema]], [[thrombocytopenia]]<ins style="font-weight: bold; text-decoration: none;"> (causing bleeding)</ins>,<ins style="font-weight: bold; text-decoration: none;"> and</ins> [[immunodeficiency]]</div></td> </tr> <tr> <td colspan="2" class="diff-empty diff-side-deleted"></td> <td class="diff-marker" data-marker="+"></td> <td style="color: #202122; 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>** Immunodeficiency is characterized by recurrent infections with encapsulated organisms and recurrent sinopulmonary infections</div></td> </tr> <tr> <td colspan="2" class="diff-empty diff-side-deleted"></td> <td class="diff-marker" data-marker="+"></td> <td style="color: #202122; 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>** Myeloid cells have impaired phagocytosis and chemotaxis; also have issues with T cell and B cell dysfunction</div></td> </tr> <tr> <td class="diff-marker"></td> <td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br /></td> <td class="diff-marker"></td> <td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br /></td> </tr> <tr> <td class="diff-marker"></td> <td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>[[Category:Genetic syndromes]]</div></td> <td class="diff-marker"></td> <td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>[[Category:Genetic syndromes]]</div></td> </tr> </table>

Aidan https://idwiki.org/index.php?title=Wiskott-Aldrich_syndrome&diff=10892&oldid=prev 2024-10-11T13:45:14Z

<p>Created page with &quot;* <a href="/Primary_immunodeficiency" title="Primary immunodeficiency">Primary immunodeficiency</a> * X-linked recessive defect in the WAS gene located at xP 11.22-23 * Characterized by <a href="/index.php?title=Eczema&amp;action=edit&amp;redlink=1" class="new" title="Eczema (page does not exist)">eczema</a>, <a href="/Thrombocytopenia" title="Thrombocytopenia">thrombocytopenia</a>, <a href="/Immunodeficiency" title="Immunodeficiency">immunodeficiency</a> <a href="/index.php?title=Category:Genetic_syndromes&amp;action=edit&amp;redlink=1" class="new" title="Category:Genetic syndromes (page does not exist)">Category:Genetic syndromes</a> <a href="/index.php?title=Category:Immunodeficiencies&amp;action=edit&amp;redlink=1" class="new" title="Category:Immunodeficiencies (page does not exist)">Category:Immunodeficiencies</a>&quot;</p> <p><b>New page</b></p><div>* [[Primary immunodeficiency]]<br /> * X-linked recessive defect in the WAS gene located at xP 11.22-23<br /> * Characterized by [[eczema]], [[thrombocytopenia]], [[immunodeficiency]]<br /> <br /> [[Category:Genetic syndromes]]<br /> [[Category:Immunodeficiencies]]</div>

Aidan