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      <title>Genome disorder project by CARTER RAZINK</title>
      <link>https://padlet.com/91716/4pl95vgybbaf</link>
      <description></description>
      <language>en-us</language>
      <pubDate>2016-02-23 19:49:29 UTC</pubDate>
      <lastBuildDate>2023-04-16 21:20:08 UTC</lastBuildDate>
      <webMaster>hello@padlet.com</webMaster>
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         <title>Disorder Specialist</title>
         <author>32256</author>
         <link>https://padlet.com/91716/4pl95vgybbaf/wish/97116196</link>
         <description><![CDATA[<div>a. Waardenburg syndrome, Klein-Waardenburg syndrome; Waardenburg-Shah syndrome<br>b. More precisely, the&nbsp;<em>EDN3</em>&nbsp;gene is located from base pair 59,300,424 to base pair 59,325,992 on chromosome 20.<br>c. 1.Heterochromia- different colored pigments of eyes<br>&nbsp; &nbsp; 2. Constipation<br>&nbsp; &nbsp; 3. Deafness, hearing impairments<br>&nbsp; &nbsp; 4. Partial Albinism<br>&nbsp; &nbsp; 5. Wide set eyes&nbsp;<br>&nbsp; &nbsp; 6. Cleft lip<br>&nbsp; &nbsp; 7. White patch of hair or early graying of the hair<br>&nbsp; &nbsp; 8. Possible slight decrease in intellectual function<br>&nbsp; &nbsp; 9. Difficulty completely straightening joints<br>d.&nbsp; There is no specific treatment. Special diets and medicines to keep the bowel moving are prescribed to those patients who have constipation.&nbsp;<br>e. Normal life expectancy<br>f. Prenatal tests are possible for Parents to test for Waardenburg Syndrome, although they are not recommended due to the high risk of miscarriage.<br><br></div>]]></description>
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         <pubDate>2016-02-24 19:44:30 UTC</pubDate>
         <guid>https://padlet.com/91716/4pl95vgybbaf/wish/97116196</guid>
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         <title></title>
         <author>32256</author>
         <link>https://padlet.com/91716/4pl95vgybbaf/wish/97118264</link>
         <description><![CDATA[<div><figure class="attachment attachment-preview" data-trix-attachment="{&quot;contentType&quot;:&quot;image&quot;,&quot;height&quot;:172,&quot;url&quot;:&quot;https://upload.wikimedia.org/wikipedia/commons/thumb/a/af/Human_male_karyotpe_high_resolution_-_Chromosome_20.png/220px-Human_male_karyotpe_high_resolution_-_Chromosome_20.png&quot;,&quot;width&quot;:220}" data-trix-content-type="image"><img src="https://upload.wikimedia.org/wikipedia/commons/thumb/a/af/Human_male_karyotpe_high_resolution_-_Chromosome_20.png/220px-Human_male_karyotpe_high_resolution_-_Chromosome_20.png" width="220" height="172"><figcaption class="caption"></figcaption></figure></div>]]></description>
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         <pubDate>2016-02-24 19:51:03 UTC</pubDate>
         <guid>https://padlet.com/91716/4pl95vgybbaf/wish/97118264</guid>
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      <item>
         <title>Works Cited</title>
         <author>32256</author>
         <link>https://padlet.com/91716/4pl95vgybbaf/wish/97635956</link>
         <description><![CDATA[<div>"Waardenburg Syndrome: MedlinePlus Medical Encyclopedia."&nbsp;<em>U.S National Library of&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; Medicine</em>. U.S. National Library of Medicine, n.d. Web. 26 Feb. 2016.<br>&nbsp;"Waardenburg Syndrome - NORD (National Organization for Rare Disorders)."&nbsp;<em>NORD&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;(National Organization for Rare Disorders)</em>. N.p., n.d. Web. 26 Feb. 2016.<br>&nbsp;"Waardenburg Syndrome."&nbsp;<em>WebMD</em>. WebMD, n.d. Web. 26 Feb. 2016.<br>Waardenburg Syndrome."&nbsp;<em>Genetics Home Reference</em>. N.p., n.d. Web. 26 Feb. 2016.<br><em>Wikipedia</em>. Wikimedia Foundation, n.d. Web. 26 Feb. 2016.<br>"Genetics of Waardenburg Syndrome."&nbsp;<em>: Overview, Gene Mutations</em>. N.p., n.d. Web. 26&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Feb. 2016.<br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2016-02-26 19:13:31 UTC</pubDate>
         <guid>https://padlet.com/91716/4pl95vgybbaf/wish/97635956</guid>
      </item>
      <item>
         <title>Genetic Counselor #1 </title>
         <author>91716</author>
         <link>https://padlet.com/91716/4pl95vgybbaf/wish/97638920</link>
         <description><![CDATA[<div>Waardenburg Syndrome is a polygenic mutation that is purely based on genetic factors alone. Waardensburg Syndrome arose from genetic mutations. It is an autosomal dominant trait. (Wikipedia 1)</div>]]></description>
         <enclosure url="" />
         <pubDate>2016-02-26 19:23:36 UTC</pubDate>
         <guid>https://padlet.com/91716/4pl95vgybbaf/wish/97638920</guid>
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         <title>Genetic Counselor #2</title>
         <author>91716</author>
         <link>https://padlet.com/91716/4pl95vgybbaf/wish/97639400</link>
         <description><![CDATA[<div>Rarity is between 1/42000-50000 people. All ages and sexes are affected equally. I would show them all of the possible side affects of the disease and show them the odds of their child having this defect. (Genetics 1)<br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2016-02-26 19:25:16 UTC</pubDate>
         <guid>https://padlet.com/91716/4pl95vgybbaf/wish/97639400</guid>
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         <title>Genetic Counselor #3</title>
         <author>91716</author>
         <link>https://padlet.com/91716/4pl95vgybbaf/wish/97640369</link>
         <description><![CDATA[<div>B = Waardenburgs<br>b = Normal<br>(Mutations 1)</div>]]></description>
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         <pubDate>2016-02-26 19:29:01 UTC</pubDate>
         <guid>https://padlet.com/91716/4pl95vgybbaf/wish/97640369</guid>
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      <item>
         <title>Disorder Specialist #1</title>
         <author>91716</author>
         <link>https://padlet.com/91716/4pl95vgybbaf/wish/97642197</link>
         <description><![CDATA[<div>There are multiple names for Waardenburg syndrome. They include Klein-Waardenburg syndrome and Waardenburg-Shah syndrome. More precisely, the <em>EDN3</em> gene is located from base pair 59,300,424 to base pair 59,325,992 on chromosome 20. (NORD 1)<br><br></div>]]></description>
         <enclosure url="https://upload.wikimedia.org/wikipedia/commons/thumb/a/af/Human_male_karyotpe_high_resolution_-_Chromosome_20.png/220px-Human_male_karyotpe_high_resolution_-_Chromosome_20.png" />
         <pubDate>2016-02-26 19:36:28 UTC</pubDate>
         <guid>https://padlet.com/91716/4pl95vgybbaf/wish/97642197</guid>
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      <item>
         <title>Disorder Specialist #2</title>
         <author>91716</author>
         <link>https://padlet.com/91716/4pl95vgybbaf/wish/97642416</link>
         <description><![CDATA[<div>c. 1.Heterochromia- different colored pigments of eyes<br>&nbsp; &nbsp; 2. Constipation<br>&nbsp; &nbsp; 3. Deafness, hearing impairments<br>&nbsp; &nbsp; 4. Partial Albinism<br>&nbsp; &nbsp; 5. Wide set eyes&nbsp;<br>&nbsp; &nbsp; 6. Cleft lip<br>&nbsp; &nbsp; 7. White patch of hair or early graying of the hair<br>&nbsp; &nbsp; 8. Possible slight decrease in intellectual function<br>&nbsp; &nbsp; 9. Difficulty completely straightening joints<br>d.&nbsp; There is no specific treatment. Special diets and medicines to keep the bowel moving are prescribed to those patients who have constipation. (Medicine 1)<br><a href="https://padlet-res.cloudinary.com/image/fetch/a_exif,c_limit,dpr_1.0,f_auto,fl_lossy,w_720/http%3A%2F%2Fghr.nlm.nih.gov%2FdynamicImages%2Fchromomap%2FEDN3.jpeg">%3A%2F%2Fghr.nlm.nih.gov%2FdynamicImages%2Fchromomap%2FEDN3.jpeg</a></div>]]></description>
         <enclosure url="http://ghr.nlm.nih.gov/dynamicImages/chromomap/EDN3.jpeg" />
         <pubDate>2016-02-26 19:37:21 UTC</pubDate>
         <guid>https://padlet.com/91716/4pl95vgybbaf/wish/97642416</guid>
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      <item>
         <title>Disorder Specialist #3</title>
         <author>91716</author>
         <link>https://padlet.com/91716/4pl95vgybbaf/wish/97643940</link>
         <description><![CDATA[<div>People with Waardensburg have a normal life expectancy. Prenatal tests are possible for Parents to test for Waardenburg Syndrome, although they are not recommended due to the high risk of miscarriage.</div>]]></description>
         <enclosure url="" />
         <pubDate>2016-02-26 19:40:04 UTC</pubDate>
         <guid>https://padlet.com/91716/4pl95vgybbaf/wish/97643940</guid>
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