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      <title>fragile x by Ryan Whitener</title>
      <link>https://padlet.com/ryanytner/FragileXSyndromeRyanWhitener</link>
      <description>Made with the help of a typing monkey</description>
      <language>en-us</language>
      <pubDate>2017-04-21 02:25:02 UTC</pubDate>
      <lastBuildDate>2025-11-01 16:14:21 UTC</lastBuildDate>
      <webMaster>hello@padlet.com</webMaster>
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         <title>Support</title>
         <author>ryanytner</author>
         <link>https://padlet.com/ryanytner/FragileXSyndromeRyanWhitener/wish/167409643</link>
         <description><![CDATA[]]></description>
         <enclosure url="https://www.fragilex.org.au" />
         <pubDate>2017-04-21 02:59:40 UTC</pubDate>
         <guid>https://padlet.com/ryanytner/FragileXSyndromeRyanWhitener/wish/167409643</guid>
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      <item>
         <title>Video explanation</title>
         <author>ryanytner</author>
         <link>https://padlet.com/ryanytner/FragileXSyndromeRyanWhitener/wish/167410007</link>
         <description><![CDATA[]]></description>
         <enclosure url="https://www.youtube.com/watch?v=9_PEW6ocSNs" />
         <pubDate>2017-04-21 03:05:27 UTC</pubDate>
         <guid>https://padlet.com/ryanytner/FragileXSyndromeRyanWhitener/wish/167410007</guid>
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      <item>
         <title>Where it comes from</title>
         <author>ryanytner</author>
         <link>https://padlet.com/ryanytner/FragileXSyndromeRyanWhitener/wish/167410031</link>
         <description><![CDATA[<div>The fmr1 gene responsible for producing a protein vital for normal brain development. This is normally made of up to 44 repeats of the cgg sequence in the gene. Some people with this gene may contain from 55-200 repeats making them a carrier. This is a fragile x pre mutation aka a carrier who is unaffected. in someone with over 200 repeats this stops the fmr1 gene from producing its necessary protein for proper brain growth.</div>]]></description>
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         <pubDate>2017-04-21 03:05:50 UTC</pubDate>
         <guid>https://padlet.com/ryanytner/FragileXSyndromeRyanWhitener/wish/167410031</guid>
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      <item>
         <title>The worlds most common inherited cause of mental imparement</title>
         <author>ryanytner</author>
         <link>https://padlet.com/ryanytner/FragileXSyndromeRyanWhitener/wish/167410371</link>
         <description><![CDATA[]]></description>
         <enclosure url="" />
         <pubDate>2017-04-21 03:11:24 UTC</pubDate>
         <guid>https://padlet.com/ryanytner/FragileXSyndromeRyanWhitener/wish/167410371</guid>
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      <item>
         <title>How its passes down</title>
         <author>ryanytner</author>
         <link>https://padlet.com/ryanytner/FragileXSyndromeRyanWhitener/wish/167410983</link>
         <description><![CDATA[<div>If a male carrier has a daughter with an unaffected female she will have the gene but only be a carrier. if the same people have a son the son will always be unaffected. If an unaffected male and carrier female have a child then the children, male of female will have a 50% chance of being affected either carrier or actually having it.</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-04-21 03:19:17 UTC</pubDate>
         <guid>https://padlet.com/ryanytner/FragileXSyndromeRyanWhitener/wish/167410983</guid>
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      <item>
         <title>Symptoms in general</title>
         <author>ryanytner</author>
         <link>https://padlet.com/ryanytner/FragileXSyndromeRyanWhitener/wish/167411417</link>
         <description><![CDATA[<div>learning disabilities<br>cognitive impairment<br>autistic behaviors<br>hyperactivity<br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2017-04-21 03:25:20 UTC</pubDate>
         <guid>https://padlet.com/ryanytner/FragileXSyndromeRyanWhitener/wish/167411417</guid>
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      <item>
         <title>Symptoms to look for in infants</title>
         <author>ryanytner</author>
         <link>https://padlet.com/ryanytner/FragileXSyndromeRyanWhitener/wish/167412497</link>
         <description><![CDATA[<div>poor muscle tone<br>gastric reflex<br>common ear infections<br>crawling, walking, and talking delayed development.</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-04-21 03:37:51 UTC</pubDate>
         <guid>https://padlet.com/ryanytner/FragileXSyndromeRyanWhitener/wish/167412497</guid>
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      <item>
         <title>1:35-2:35 gives visual explatation</title>
         <author>ryanytner</author>
         <link>https://padlet.com/ryanytner/FragileXSyndromeRyanWhitener/wish/167412712</link>
         <description><![CDATA[]]></description>
         <enclosure url="https://www.youtube.com/watch?v=2QB6nV-IRtQ" />
         <pubDate>2017-04-21 03:40:21 UTC</pubDate>
         <guid>https://padlet.com/ryanytner/FragileXSyndromeRyanWhitener/wish/167412712</guid>
      </item>
      <item>
         <title>Family and how they got through it</title>
         <author>ryanytner</author>
         <link>https://padlet.com/ryanytner/FragileXSyndromeRyanWhitener/wish/167412946</link>
         <description><![CDATA[<div>IIt takes a lot of patience, time and attention. Lots of therapy home and professional can help someone with fragile x to speak and do some small semi normal things.</div>]]></description>
         <enclosure url="https://www.youtube.com/watch?v=QrWu4ncrDyg&amp;t=1s" />
         <pubDate>2017-04-21 03:43:19 UTC</pubDate>
         <guid>https://padlet.com/ryanytner/FragileXSyndromeRyanWhitener/wish/167412946</guid>
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