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	<title>CatsWannaBeCats.Com | Fitzpatrick Brogaard | Activity</title>
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				<title>Fitzpatrick Brogaard posted an update: Gorlin syndrome is an autosomal dominant inherited condition [&#133;]</title>
				<link>https://www.catswannabecats.com/activity/p/9389/</link>
				<pubDate>Sat, 31 May 2025 22:37:46 -0400</pubDate>

									<content:encoded><![CDATA[<p>Gorlin syndrome is an autosomal dominant inherited condition that exhibits high penetrance and variable expressivity. The syndrome is caused by mutations in PTCH, a tumor suppressor gene that has been mapped to chromosome 9q22.3-q31. It is observed that most aggressive forms of keratocystic odontogenic tumor are the first signs of this syndrome&hellip;<span class="activity-read-more" id="activity-read-more-9389"><a href="https://www.catswannabecats.com/activity/p/9389/" rel="nofollow ugc">[Read more]</a></span></p>
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				<title>Fitzpatrick Brogaard became a registered member</title>
				<link>https://www.catswannabecats.com/activity/p/7698/</link>
				<pubDate>Sat, 31 May 2025 19:48:16 -0400</pubDate>

				
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