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      <title>Noonan Syndrome by Casper1777 FTW</title>
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      <description></description>
      <language>en-us</language>
      <pubDate>2018-03-22 13:02:39 UTC</pubDate>
      <lastBuildDate>2018-03-22 13:44:58 UTC</lastBuildDate>
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         <title>Description of disease</title>
         <author>shuffmenard</author>
         <link>https://padlet.com/shuffmenard/o4vv7kjoraiy/wish/244966385</link>
         <description><![CDATA[<div>Noonan syndrome is a disorder that involves unusual facial characteristics, short stature, heart defects present at birth, bleeding problems, developmental delays, and malformations of the bones of the rib cage.<br><br><br></div>]]></description>
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         <pubDate>2018-03-22 13:07:29 UTC</pubDate>
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         <title>Initial Symptoms</title>
         <author>shuffmenard</author>
         <link>https://padlet.com/shuffmenard/o4vv7kjoraiy/wish/244967050</link>
         <description><![CDATA[<ul><li>A characteristic facial appearance.</li><li>Short stature.</li><li>Heart defect present at birth (congenital heart defect).</li><li>A broad or webbed neck.</li><li>Minor eye problems such as strabismus in up to 95 percent of individuals.</li><li>Bleeding problems such as a history of abnormal bleeding or bruising.</li><li>An unusual chest shape with widely-spaced and low set nipples.</li><li>Developmental delay of varying degrees, but usually mild.</li><li>In males, undescended testes (cryptorchidism).</li></ul><div><br><br></div><div><br></div>]]></description>
         <enclosure url="http://www.genome.gov/25521674/learning-about-noonan-syndrome/." />
         <pubDate>2018-03-22 13:08:52 UTC</pubDate>
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