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      <title>Cystic fibrosis by Yasser  Omar</title>
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      <language>en-us</language>
      <pubDate>2018-02-14 20:09:19 UTC</pubDate>
      <lastBuildDate>2018-02-26 20:18:20 UTC</lastBuildDate>
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         <author>sc995418</author>
         <link>https://padlet.com/sc995418/smuhn2wc5dhy/wish/232112806</link>
         <description><![CDATA[<ol><li>a hereditary disorder affecting the exocrine glands. It causes the production of abnormally thick mucus, leading to the blockage of the pancreatic ducts, intestines, and bronchi and often resulting in respiratory infection.</li></ol><div><br></div>]]></description>
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         <pubDate>2018-02-15 19:34:46 UTC</pubDate>
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         <title></title>
         <author>sc995418</author>
         <link>https://padlet.com/sc995418/smuhn2wc5dhy/wish/232116214</link>
         <description><![CDATA[<div>the mucus clogs the airways and traps bacteria leading to infections, extensive lung damage, and eventually, respiratory failure. </div>]]></description>
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         <pubDate>2018-02-15 19:40:34 UTC</pubDate>
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         <author>sc995418</author>
         <link>https://padlet.com/sc995418/smuhn2wc5dhy/wish/232122260</link>
         <description><![CDATA[<div>People with CF can have a variety of symptoms, including. </div><ul><li>Very salty-tasting skin.</li><li>Persistent coughing, at times with phlegm.</li><li>Persistent coughing, at times with phlegm.</li><li>Wheezing or shortness of breath.</li><li>Poor growth or weight gain in spite of a good appetite.</li><li>Poor growth or weight gain in spite of a good appetite.</li></ul>]]></description>
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         <pubDate>2018-02-15 19:51:42 UTC</pubDate>
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         <title></title>
         <author>sc995418</author>
         <link>https://padlet.com/sc995418/smuhn2wc5dhy/wish/232123217</link>
         <description><![CDATA[<div>Both parents must have at least one copy of the defective gene. People with only one copy of the defective CF gene are called carriers, but they do not have the disease.</div>]]></description>
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         <pubDate>2018-02-15 19:53:31 UTC</pubDate>
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         <title></title>
         <author>sc995418</author>
         <link>https://padlet.com/sc995418/smuhn2wc5dhy/wish/232127398</link>
         <description><![CDATA[<div>The defective CF gene contains a slight abnormality called mutation. </div>]]></description>
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         <pubDate>2018-02-15 20:01:16 UTC</pubDate>
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         <title></title>
         <author>sc995418</author>
         <link>https://padlet.com/sc995418/smuhn2wc5dhy/wish/232130458</link>
         <description><![CDATA[<div>There are more than 1,700 known mutations of the disease.    <br>Most genetic tests only screen for the most common CF mutations. </div>]]></description>
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         <pubDate>2018-02-15 20:07:47 UTC</pubDate>
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         <title></title>
         <author>sc995418</author>
         <link>https://padlet.com/sc995418/smuhn2wc5dhy/wish/232133191</link>
         <description><![CDATA[<div>Cystic fibrosis is a complex disease and the types and severity of symptoms can differ widely from person to person. </div>]]></description>
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         <pubDate>2018-02-15 20:13:26 UTC</pubDate>
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         <title></title>
         <author>sc995418</author>
         <link>https://padlet.com/sc995418/smuhn2wc5dhy/wish/232135187</link>
         <description><![CDATA[<div>People with cystic fibrosis are at greater risk of getting lung infections because thick, sticky mucus builds up in their lungs, allowing germs to thrive and multiply. </div>]]></description>
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         <pubDate>2018-02-15 20:17:37 UTC</pubDate>
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