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      <title>cystic fibrosis by Breanna Jefferson</title>
      <link>https://padlet.com/breannaj7103/Bookmarks</link>
      <description>genetic disorder project</description>
      <language>en-us</language>
      <pubDate>2020-11-11 15:47:48 UTC</pubDate>
      <lastBuildDate>2025-12-28 07:03:30 UTC</lastBuildDate>
      <webMaster>hello@padlet.com</webMaster>
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         <title></title>
         <author>breannaj7103</author>
         <link>https://padlet.com/breannaj7103/Bookmarks/wish/913285794</link>
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         <pubDate>2020-11-11 15:58:17 UTC</pubDate>
         <guid>https://padlet.com/breannaj7103/Bookmarks/wish/913285794</guid>
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         <title>Life With Cystic Fibrosis</title>
         <author>breannaj7103</author>
         <link>https://padlet.com/breannaj7103/Bookmarks/wish/913298959</link>
         <description><![CDATA[<div>People with CF will have quite a young life expectancy, typically anywhere between 31-45 years old.</div>]]></description>
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         <pubDate>2020-11-11 16:01:33 UTC</pubDate>
         <guid>https://padlet.com/breannaj7103/Bookmarks/wish/913298959</guid>
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         <title>What Causes Cystic Fibrosis?</title>
         <author>breannaj7103</author>
         <link>https://padlet.com/breannaj7103/Bookmarks/wish/913323691</link>
         <description><![CDATA[<div><strong>CHROMOSOMAL MUTATION</strong>-alterations that affect whole chromosomes and whole genes.<br><br>If you have CF that means chromosome #7 out of 21 was affected.</div>]]></description>
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         <pubDate>2020-11-11 16:07:34 UTC</pubDate>
         <guid>https://padlet.com/breannaj7103/Bookmarks/wish/913323691</guid>
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         <title>Visible Traits</title>
         <author>breannaj7103</author>
         <link>https://padlet.com/breannaj7103/Bookmarks/wish/913391041</link>
         <description><![CDATA[<div>there are actually very little to none visible traits. you may experience poor growth or weight loss/gain, but nothing to visible for a person to know you have CF.<br><br>There are no unique features of individuals with this disorder.</div><div><br></div>]]></description>
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         <pubDate>2020-11-11 16:24:30 UTC</pubDate>
         <guid>https://padlet.com/breannaj7103/Bookmarks/wish/913391041</guid>
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         <title>Affect On Bodily Functions</title>
         <author>breannaj7103</author>
         <link>https://padlet.com/breannaj7103/Bookmarks/wish/913405148</link>
         <description><![CDATA[<div>Cystic fibrosis causes thick mucus that clogs certain organs (lungs, pancreas, intestines). This can cause issues with your lungs and digestive system.</div>]]></description>
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         <pubDate>2020-11-11 16:28:10 UTC</pubDate>
         <guid>https://padlet.com/breannaj7103/Bookmarks/wish/913405148</guid>
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         <title>Treatments For Cystic Fibrosis</title>
         <author>breannaj7103</author>
         <link>https://padlet.com/breannaj7103/Bookmarks/wish/913443723</link>
         <description><![CDATA[<ul><li>medications that target gene mutations</li><li>airway clearance techniques (also called chest physical therapy)</li><li>pulmonary rehabilitation</li><li>surgical and other procedures</li></ul><div><br></div>]]></description>
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         <pubDate>2020-11-11 16:38:05 UTC</pubDate>
         <guid>https://padlet.com/breannaj7103/Bookmarks/wish/913443723</guid>
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         <title>How Is This Disorder Inherited?</title>
         <author>breannaj7103</author>
         <link>https://padlet.com/breannaj7103/Bookmarks/wish/913456327</link>
         <description><![CDATA[<div>In order to have cystic fibrosis you must have inherited two copies of the gene (one copy from each parent). Both parents must have at least one copy of the defective gene for their kid to inherit it.</div>]]></description>
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         <pubDate>2020-11-11 16:41:18 UTC</pubDate>
         <guid>https://padlet.com/breannaj7103/Bookmarks/wish/913456327</guid>
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         <title>Can A Person Be A Carrier?</title>
         <author>breannaj7103</author>
         <link>https://padlet.com/breannaj7103/Bookmarks/wish/913467208</link>
         <description><![CDATA[Yes a person can be a carrier but not have cystic fibrosis. You must have two copies of the cystic fibrosis gene, so the people who only have one copy of the cystic fibrosis gene are called carriers, but do not actually have the disorder.]]></description>
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         <pubDate>2020-11-11 16:44:16 UTC</pubDate>
         <guid>https://padlet.com/breannaj7103/Bookmarks/wish/913467208</guid>
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         <title>Other Info On Heredity</title>
         <author>breannaj7103</author>
         <link>https://padlet.com/breannaj7103/Bookmarks/wish/913507844</link>
         <description><![CDATA[<div>Genetic testing can be used to tell if a person carries a mutation of the cystic fibrosis gene.</div>]]></description>
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         <pubDate>2020-11-11 16:54:29 UTC</pubDate>
         <guid>https://padlet.com/breannaj7103/Bookmarks/wish/913507844</guid>
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         <title></title>
         <author>breannaj7103</author>
         <link>https://padlet.com/breannaj7103/Bookmarks/wish/913521733</link>
         <description><![CDATA[]]></description>
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         <pubDate>2020-11-11 16:58:05 UTC</pubDate>
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         <title></title>
         <author>breannaj7103</author>
         <link>https://padlet.com/breannaj7103/Bookmarks/wish/913535808</link>
         <description><![CDATA[]]></description>
         <enclosure url="https://www.cff.org/What-is-CF/About-Cystic-Fibrosis/" />
         <pubDate>2020-11-11 17:01:57 UTC</pubDate>
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         <title></title>
         <author>breannaj7103</author>
         <link>https://padlet.com/breannaj7103/Bookmarks/wish/913541924</link>
         <description><![CDATA[]]></description>
         <enclosure url="https://www.mayoclinic.org/diseases-conditions/cystic-fibrosis/diagnosis-treatment/drc-20353706" />
         <pubDate>2020-11-11 17:03:43 UTC</pubDate>
         <guid>https://padlet.com/breannaj7103/Bookmarks/wish/913541924</guid>
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         <title></title>
         <author>breannaj7103</author>
         <link>https://padlet.com/breannaj7103/Bookmarks/wish/913546026</link>
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         <enclosure url="https://www.nhlbi.nih.gov/health-topics/cystic-fibrosis" />
         <pubDate>2020-11-11 17:04:52 UTC</pubDate>
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