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      <title>My distinguished padlet by malaik</title>
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      <description>malaik&#39;s padlet</description>
      <language>en-us</language>
      <pubDate>2016-11-14 18:20:42 UTC</pubDate>
      <lastBuildDate>2026-02-01 13:56:22 UTC</lastBuildDate>
      <webMaster>hello@padlet.com</webMaster>
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         <title>tay sacs</title>
         <author>malaikm13</author>
         <link>https://padlet.com/malaikm13/g76xzgisw6wt/wish/137490972</link>
         <description><![CDATA[<div>an inherited metabolic disorder in which certain lipids accumulate in the brain, causing spasticity and death in childhood. Recessive<br><a href="https://www.youtube.com/watch?v=ufEXHKqKDXk">https://www.youtube.com/watch?v=ufEXHKqKDXk</a><br><figure class="attachment attachment-preview" data-trix-attachment="{&quot;contentType&quot;:&quot;image&quot;,&quot;height&quot;:151,&quot;url&quot;:&quot;https://media.padletcdn.com/v13/image/a_exif,c_limit,dpr_auto,h_151,w_200/https%3A%2F%2Fpadlet-uploads.s3.amazonaws.com%2Fprod%2F148333042%2Fde3f97cd6d00dd6ef2d623e1cdc240f9%2FRecessive_Inheritance_new.jpg&quot;,&quot;width&quot;:199}" data-trix-content-type="image"><img src="https://media.padletcdn.com/v13/image/a_exif,c_limit,dpr_auto,h_151,w_200/https%3A%2F%2Fpadlet-uploads.s3.amazonaws.com%2Fprod%2F148333042%2Fde3f97cd6d00dd6ef2d623e1cdc240f9%2FRecessive_Inheritance_new.jpg" width="199" height="151"><figcaption class="caption"></figcaption></figure></div>]]></description>
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         <pubDate>2016-11-14 18:27:11 UTC</pubDate>
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         <title>huntington&#39;s diease</title>
         <author>malaikm13</author>
         <link>https://padlet.com/malaikm13/g76xzgisw6wt/wish/137495782</link>
         <description><![CDATA[<div>a hereditary disease marked by degeneration of the brain cells and causing chorea and progressive dementia. recessive<br><a href="https://www.youtube.com/watch?v=8lItaU0ftK8">https://www.youtube.com/watch?v=8lItaU0ftK8</a></div><div><figure class="attachment attachment-preview" data-trix-attachment="{&quot;contentType&quot;:&quot;image&quot;,&quot;height&quot;:112,&quot;url&quot;:&quot;https://media.padletcdn.com/v13/image/a_exif,c_limit,dpr_auto,h_112,w_200/https%3A%2F%2Fpadlet-uploads.s3.amazonaws.com%2Fprod%2F148333042%2Fa2770e1ab52ce8680b63ebb3a541c976%2F_83094631_p3320125_human_brain.gif&quot;,&quot;width&quot;:199}" data-trix-content-type="image"><img src="https://media.padletcdn.com/v13/image/a_exif,c_limit,dpr_auto,h_112,w_200/https%3A%2F%2Fpadlet-uploads.s3.amazonaws.com%2Fprod%2F148333042%2Fa2770e1ab52ce8680b63ebb3a541c976%2F_83094631_p3320125_human_brain.gif" width="199" height="112"><figcaption class="caption"></figcaption></figure></div>]]></description>
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         <pubDate>2016-11-14 18:37:05 UTC</pubDate>
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         <title>sickle cell anemia</title>
         <author>malaikm13</author>
         <link>https://padlet.com/malaikm13/g76xzgisw6wt/wish/137502262</link>
         <description><![CDATA[<div>a severe hereditary form of anemia in which a mutated form of hemoglobin distorts the red blood cells into a crescent shape at low oxygen levels. It is most common among those of African descent. Dominant <br><figure class="attachment attachment-preview" data-trix-attachment="{&quot;contentType&quot;:&quot;image&quot;,&quot;height&quot;:138,&quot;url&quot;:&quot;https://media.padletcdn.com/v13/image/a_exif,c_limit,dpr_auto,h_138,w_200/https%3A%2F%2Fpadlet-uploads.s3.amazonaws.com%2Fprod%2F148333042%2Fe574e64bc02ec6a12e67a05f96f55d37%2Fdownload__3_.jpg&quot;,&quot;width&quot;:199}" data-trix-content-type="image"><img src="https://media.padletcdn.com/v13/image/a_exif,c_limit,dpr_auto,h_138,w_200/https%3A%2F%2Fpadlet-uploads.s3.amazonaws.com%2Fprod%2F148333042%2Fe574e64bc02ec6a12e67a05f96f55d37%2Fdownload__3_.jpg" width="199" height="138"><figcaption class="caption"></figcaption></figure></div>]]></description>
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         <pubDate>2016-11-14 18:49:53 UTC</pubDate>
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         <title>PKU disease</title>
         <author>malaikm13</author>
         <link>https://padlet.com/malaikm13/g76xzgisw6wt/wish/137506488</link>
         <description><![CDATA[<div>&nbsp;The <strong>disease PKU</strong> is clearly inherited as a <strong>recessive</strong> trait. Only if one inherits a mutant allele from each parent will one develop the <strong>disease</strong>. However, heterozygous people are easily distinguished from homozygotes by the phenylalanine tolerance test.<br><a href="https://www.youtube.com/watch?v=uS2mpCuUJa4">https://www.youtube.com/watch?v=uS2mpCuUJa4</a><br><figure class="attachment attachment-preview" data-trix-attachment="{&quot;contentType&quot;:&quot;image&quot;,&quot;height&quot;:148,&quot;url&quot;:&quot;https://media.padletcdn.com/v13/image/a_exif,c_limit,dpr_auto,h_148,w_200/https%3A%2F%2Fpadlet-uploads.s3.amazonaws.com%2Fprod%2F148333042%2F0187d13b72fa50a46ad51f176df14e28%2FPhenylketonuria_Disease2.jpg&quot;,&quot;width&quot;:200}" data-trix-content-type="image"><img src="https://media.padletcdn.com/v13/image/a_exif,c_limit,dpr_auto,h_148,w_200/https%3A%2F%2Fpadlet-uploads.s3.amazonaws.com%2Fprod%2F148333042%2F0187d13b72fa50a46ad51f176df14e28%2FPhenylketonuria_Disease2.jpg" width="200" height="148"><figcaption class="caption"></figcaption></figure></div>]]></description>
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         <pubDate>2016-11-14 18:57:35 UTC</pubDate>
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         <title>hemophilia</title>
         <author>malaikm13</author>
         <link>https://padlet.com/malaikm13/g76xzgisw6wt/wish/137542874</link>
         <description><![CDATA[<div>a medical condition in which the ability of the blood to clot is severely reduced, causing the sufferer to bleed severely from even a slight injury. The condition is typically caused by a hereditary lack of a coagulation factor. Dominant&nbsp;<br><figure class="attachment attachment-preview" data-trix-attachment="{&quot;contentType&quot;:&quot;image&quot;,&quot;height&quot;:200,&quot;url&quot;:&quot;https://media.padletcdn.com/v13/image/a_exif,c_limit,dpr_auto,h_200,w_200/https%3A%2F%2Fpadlet-uploads.s3.amazonaws.com%2Fprod%2F148333042%2F92ade10882c6c4d8fedc40dd7eb498a7%2Fblood_clot_formation.jpeg&quot;,&quot;width&quot;:200}" data-trix-content-type="image"><img src="https://media.padletcdn.com/v13/image/a_exif,c_limit,dpr_auto,h_200,w_200/https%3A%2F%2Fpadlet-uploads.s3.amazonaws.com%2Fprod%2F148333042%2F92ade10882c6c4d8fedc40dd7eb498a7%2Fblood_clot_formation.jpeg" width="200" height="200"><figcaption class="caption"></figcaption></figure></div>]]></description>
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         <pubDate>2016-11-14 20:22:09 UTC</pubDate>
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         <title>cystic fibrosis</title>
         <author>malaikm13</author>
         <link>https://padlet.com/malaikm13/g76xzgisw6wt/wish/137545475</link>
         <description><![CDATA[<div>a hereditary disorder affecting the endocrine 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.<br><figure class="attachment attachment-preview" data-trix-attachment="{&quot;contentType&quot;:&quot;image&quot;,&quot;height&quot;:240,&quot;url&quot;:&quot;https://media.padletcdn.com/v13/image/a_exif,c_limit,dpr_auto,h_240,w_200/https%3A%2F%2Fpadlet-uploads.s3.amazonaws.com%2Fprod%2F148333042%2Fcedad4c9c659207d0538b8525c47fd0d%2Fgggg.jpg&quot;,&quot;width&quot;:199}" data-trix-content-type="image"><img src="https://media.padletcdn.com/v13/image/a_exif,c_limit,dpr_auto,h_240,w_200/https%3A%2F%2Fpadlet-uploads.s3.amazonaws.com%2Fprod%2F148333042%2Fcedad4c9c659207d0538b8525c47fd0d%2Fgggg.jpg" width="199" height="240"><figcaption class="caption"></figcaption></figure></div>]]></description>
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         <pubDate>2016-11-14 20:30:10 UTC</pubDate>
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         <title></title>
         <author>malaikm13</author>
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         <pubDate>2016-11-14 20:46:39 UTC</pubDate>
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