<?xml version="1.0"?>
<rss version="2.0">
   <channel>
      <title>Angelman Syndrome by Hope westman</title>
      <link>https://padlet.com/hopew2019/let7mo3ecrzp</link>
      <description></description>
      <language>en-us</language>
      <pubDate>2018-03-29 00:24:32 UTC</pubDate>
      <lastBuildDate>2026-02-27 00:53:55 UTC</lastBuildDate>
      <webMaster>hello@padlet.com</webMaster>
      <image>
         <url></url>
      </image>
      <item>
         <title></title>
         <author>hopew2019</author>
         <link>https://padlet.com/hopew2019/let7mo3ecrzp/wish/247109142</link>
         <description><![CDATA[<div>Angelman Syndrome is a complex genetic disorder that primarily affects the nervous system. Children with the disease are typically happy, hyperactive, and have a short attention span. It is common for the child to have a fascination with water, and find it difficult to sleep. With age, sleeping problems tend to improve. Throughout their lives severe speech impairment, seizures, and intellectual disability continue. Adults with the disease may have distinctive facial features. Common features are very fair skin and light hair, may have scolliosis. Life expectancy is normal.</div>]]></description>
         <enclosure url="" />
         <pubDate>2018-03-29 00:29:04 UTC</pubDate>
         <guid>https://padlet.com/hopew2019/let7mo3ecrzp/wish/247109142</guid>
      </item>
      <item>
         <title></title>
         <author>hopew2019</author>
         <link>https://padlet.com/hopew2019/let7mo3ecrzp/wish/247110337</link>
         <description><![CDATA[<div>Initial Symptoms of Angelman Syndrome are retardation, unusually happy demeanor, Microcephaly (small head), large jaws, jerky movements, hand flapping, developmental delay, diminished speech.</div>]]></description>
         <enclosure url="" />
         <pubDate>2018-03-29 00:37:13 UTC</pubDate>
         <guid>https://padlet.com/hopew2019/let7mo3ecrzp/wish/247110337</guid>
      </item>
      <item>
         <title></title>
         <author>hopew2019</author>
         <link>https://padlet.com/hopew2019/let7mo3ecrzp/wish/247111110</link>
         <description><![CDATA[<div>Common treatments for Angelman Syndrome are speech-language therapy, physical therapy, occupational therapy, behavioral therapy, neurological services.<br>Epilepsy medicine:<br>~Brivaracetam (Briviact)<br>~Carbamazepine (Carbatrol or Tegretol)<br>~Diazepam (Valium)<br>~Lorazepam (Ativan)<br>~Clonazepam (Klonopin)<br>~Eslicarbazepine (Aptiom)</div>]]></description>
         <enclosure url="" />
         <pubDate>2018-03-29 00:42:12 UTC</pubDate>
         <guid>https://padlet.com/hopew2019/let7mo3ecrzp/wish/247111110</guid>
      </item>
      <item>
         <title></title>
         <author>hopew2019</author>
         <link>https://padlet.com/hopew2019/let7mo3ecrzp/wish/247113025</link>
         <description><![CDATA[<div>Side effects of Epilepsy medicine:<br>~Brivaracetam (Briviact)<br>side effects- drowsiness, dizziness, fatigue, nausea, and vomiting.<br>~Carbamazepine (Carbatrol or Tegretol)<br>side effects- fatigue, vision changes, nausea, dizziness, and rash.<br>~Diazepam (Valium), Lorazepam (Ativan), Clonazepam (Klonopin)<br>side effects-tiredness, unsteady walking, nausea, depression, loss of appetite.<br>~Eslicarbazepine (Aptiom)<br>side effects-dizziness, nausea, headache, vomiting, fatigue, vertigo, ataxia, blurred vision, and tremor.<br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2018-03-29 00:56:05 UTC</pubDate>
         <guid>https://padlet.com/hopew2019/let7mo3ecrzp/wish/247113025</guid>
      </item>
      <item>
         <title></title>
         <author>hopew2019</author>
         <link>https://padlet.com/hopew2019/let7mo3ecrzp/wish/247116954</link>
         <description><![CDATA[<div>Typically there is no prevention for this disease. When the disease is inherited there are certain therapy's and medication you can take to treat the disease but there is no way to prevent it.</div>]]></description>
         <enclosure url="" />
         <pubDate>2018-03-29 01:21:40 UTC</pubDate>
         <guid>https://padlet.com/hopew2019/let7mo3ecrzp/wish/247116954</guid>
      </item>
      <item>
         <title></title>
         <author>hopew2019</author>
         <link>https://padlet.com/hopew2019/let7mo3ecrzp/wish/247117838</link>
         <description><![CDATA[<div>Angelman Syndrome is associated with chromosome 15.</div>]]></description>
         <enclosure url="" />
         <pubDate>2018-03-29 01:26:43 UTC</pubDate>
         <guid>https://padlet.com/hopew2019/let7mo3ecrzp/wish/247117838</guid>
      </item>
      <item>
         <title></title>
         <author>hopew2019</author>
         <link>https://padlet.com/hopew2019/let7mo3ecrzp/wish/247118156</link>
         <description><![CDATA[<div>Angelman Syndrome is inherited when a loss of function ofagene called UBE3A on chromosome 15. Mutation in the maternal copy of the UBE3A gene. </div>]]></description>
         <enclosure url="" />
         <pubDate>2018-03-29 01:28:30 UTC</pubDate>
         <guid>https://padlet.com/hopew2019/let7mo3ecrzp/wish/247118156</guid>
      </item>
      <item>
         <title></title>
         <author>hopew2019</author>
         <link>https://padlet.com/hopew2019/let7mo3ecrzp/wish/247118544</link>
         <description><![CDATA[<div>Angelman Syndrome effects 10-15 percent of the population.</div>]]></description>
         <enclosure url="" />
         <pubDate>2018-03-29 01:30:31 UTC</pubDate>
         <guid>https://padlet.com/hopew2019/let7mo3ecrzp/wish/247118544</guid>
      </item>
      <item>
         <title></title>
         <author>hopew2019</author>
         <link>https://padlet.com/hopew2019/let7mo3ecrzp/wish/247118772</link>
         <description><![CDATA[<div>“Angelman Syndrome - Genetics Home Reference.” <em>U.S. National Library of Medicine</em>, National Institutes of Health, ghr.nlm.nih.gov/condition/angelman-syndrome.<br><br></div><div>“Symptoms of Angelman Syndrome.” <em>Symptoms of Angelman Syndrome - RightDiagnosis.com</em>, www.rightdiagnosis.com/a/angelman_syndrome/symptoms.htm.<br><br></div><div>“Pediatric Angelman Syndrome - Genetic Disorders.” <em>Children's Health</em>, www.childrens.com/specialties-services/specialty-centers-and-programs/autism-and-developmental-disabilities/conditions-and-treatments/angelman-syndrome.<br><br></div><div>“Find Out More.” <em>Aptiom</em>, www.aptiom.com/anti-seizure-medication.html?utm_source=bing&amp;utm_medium=cpc&amp;utm_term=medicine%2Bfor%2Bepilepsy&amp;utm_campaign=bs-epilepsy%2Bmedication_ex&amp;gclid=CMGDtYiAgNoCFRfQswodjp0MRQ&amp;gclsrc=ds.<br><br></div><div>“Epilepsy Drugs to Treat Seizures.” <em>WebMD</em>, WebMD, www.webmd.com/epilepsy/medications-treat-seizures#1.<br><br></div><div>“Angelman Syndrome.” <em>Genetic and Rare Diseases Information Center</em>, U.S. Department of Health and Human Services, rarediseases.info.nih.gov/diseases/5810/angelman-syndrome.<br><br>“Angelman Syndrome - Genetics Home Reference.” <em>U.S. National Library of Medicine</em>, National Institutes of Health, ghr.nlm.nih.gov/condition/angelman-syndrome<br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2018-03-29 01:31:36 UTC</pubDate>
         <guid>https://padlet.com/hopew2019/let7mo3ecrzp/wish/247118772</guid>
      </item>
      <item>
         <title></title>
         <author>hopew2019</author>
         <link>https://padlet.com/hopew2019/let7mo3ecrzp/wish/247119914</link>
         <description><![CDATA[<div><figure class="attachment attachment--preview"><img src="https://achievementcenteroftexas.org/wp-content/uploads/2018/02/Angelman-Syndrome-400x200.jpg" width="400" height="200"><figcaption class="attachment__caption"></figcaption></figure></div>]]></description>
         <enclosure url="" />
         <pubDate>2018-03-29 01:37:41 UTC</pubDate>
         <guid>https://padlet.com/hopew2019/let7mo3ecrzp/wish/247119914</guid>
      </item>
   </channel>
</rss>
