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      <title>Adrenoleukodystrophy(ALD) by Logan Keener</title>
      <link>https://padlet.com/2021logankeener/7fi2gzuamtmk</link>
      <description>It&#39;s a X chromosome linked disease. </description>
      <language>en-us</language>
      <pubDate>2017-11-16 12:50:26 UTC</pubDate>
      <lastBuildDate>2023-01-24 04:46:02 UTC</lastBuildDate>
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      <item>
         <title>Causes</title>
         <author>2021logankeener</author>
         <link>https://padlet.com/2021logankeener/7fi2gzuamtmk/wish/207639912</link>
         <description><![CDATA[<div>ALD is caused by an abnormality in the ABCD1 gene located on the X chromosome. This gene abnormality leads to the production of an abnormal ALDP protein in a part of the cell called the peroxisome, and is responsible for breaking down very long chain fatty acids. The accumulation of very long fatty acids damages the protective covering of nerves, resulting in neurological problems.</div>]]></description>
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         <pubDate>2017-11-16 13:28:38 UTC</pubDate>
         <guid>https://padlet.com/2021logankeener/7fi2gzuamtmk/wish/207639912</guid>
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         <title>Citations</title>
         <author>2021logankeener</author>
         <link>https://padlet.com/2021logankeener/7fi2gzuamtmk/wish/207640905</link>
         <description><![CDATA[<div><a href="https://rarediseases.org/rare-diseases/adrenoleukodystrophy/">https://rarediseases.org/rare-diseases/adrenoleukodystrophy/</a><br><br><a href="https://en.wikipedia.org/wiki/Adrenoleukodystrophy">Adrenoleukodystrophy. (2017, October 31). Retrieved November 17, 2017, from https://en.wikipedia.org/wiki/Adrenoleukodystrophy</a><br><a href="http://study.com/academy/lesson/peroxisomes-definition-structure-functions.html"><br>Baron, A. (n.d.). Peroxisomes: Definition, Structure &amp; Functions. Retrieved November 17, 2017, from http://study.com/academy/lesson/peroxisomes-definition-structure-functions.html</a></div>]]></description>
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         <pubDate>2017-11-16 13:30:56 UTC</pubDate>
         <guid>https://padlet.com/2021logankeener/7fi2gzuamtmk/wish/207640905</guid>
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         <title>Symptoms </title>
         <author>2021logankeener</author>
         <link>https://padlet.com/2021logankeener/7fi2gzuamtmk/wish/207642625</link>
         <description><![CDATA[<ul><li>Addison Disease with Cerebral Sclerosis</li><li>Adrenomyeloneuropathy</li><li>ALD</li><li>AMN</li><li>Bronze Schilder Disease</li><li>Melanodermic Leukodystrophy</li><li>Schilder Disease</li><li>Siemerling-Creutzfeldt Disease</li><li>Sudanophilic Leukodystrophy</li><li>X- ALD</li></ul>]]></description>
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         <pubDate>2017-11-16 13:34:54 UTC</pubDate>
         <guid>https://padlet.com/2021logankeener/7fi2gzuamtmk/wish/207642625</guid>
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         <title>Treatments</title>
         <author>2021logankeener</author>
         <link>https://padlet.com/2021logankeener/7fi2gzuamtmk/wish/207648773</link>
         <description><![CDATA[<div>The abnormal adrenal function is treated with corticosteroid replacement therapy. Bone marrow transplantation has been successful in individuals who are in the early stages of ALD. Affected individuals can benefit from supportive care from psychologists, educators, physical therapists, urologists, and family and vocational counselors. Genetic counseling is recommended for affected individuals and their family members.</div>]]></description>
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         <pubDate>2017-11-16 13:47:18 UTC</pubDate>
         <guid>https://padlet.com/2021logankeener/7fi2gzuamtmk/wish/207648773</guid>
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         <title>Peroxisome</title>
         <author>2021logankeener</author>
         <link>https://padlet.com/2021logankeener/7fi2gzuamtmk/wish/208073568</link>
         <description><![CDATA[]]></description>
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         <pubDate>2017-11-17 12:57:02 UTC</pubDate>
         <guid>https://padlet.com/2021logankeener/7fi2gzuamtmk/wish/208073568</guid>
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      <item>
         <title>What organelle is effected?</title>
         <author>2021logankeener</author>
         <link>https://padlet.com/2021logankeener/7fi2gzuamtmk/wish/208074337</link>
         <description><![CDATA[<div>ALD is caused by mutations in ABCD1, located at Xq28 and demonstrates X-linked recessive inheritance. The gene ABCD1 encodes a peroxisomal membrane transporter which is responsible for transporting very long chain fatty acid substrate into the peroxisomes for degradation.</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-11-17 12:59:07 UTC</pubDate>
         <guid>https://padlet.com/2021logankeener/7fi2gzuamtmk/wish/208074337</guid>
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         <title>How does the Peroxisome normally work?</title>
         <author>2021logankeener</author>
         <link>https://padlet.com/2021logankeener/7fi2gzuamtmk/wish/208075223</link>
         <description><![CDATA[<div>Peroxisomes have two functions: break down fatty acids to be used for forming membranes and as fuel for respiration; and transfer hydrogen from compounds to oxygen to create hydrogen peroxide and then convert hydrogen peroxide into water.</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-11-17 13:01:42 UTC</pubDate>
         <guid>https://padlet.com/2021logankeener/7fi2gzuamtmk/wish/208075223</guid>
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      <item>
         <title>Adrenoleukodystrophy</title>
         <author>2021logankeener</author>
         <link>https://padlet.com/2021logankeener/7fi2gzuamtmk/wish/208076873</link>
         <description><![CDATA[]]></description>
         <enclosure url="" />
         <pubDate>2017-11-17 13:06:12 UTC</pubDate>
         <guid>https://padlet.com/2021logankeener/7fi2gzuamtmk/wish/208076873</guid>
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