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      <title>Inheritance of Genetic Disorders (Group 4) by Heather Murray</title>
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      <language>en-us</language>
      <pubDate>2021-02-21 16:14:31 UTC</pubDate>
      <lastBuildDate>2023-03-08 16:36:51 UTC</lastBuildDate>
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         <title>Sex-linked</title>
         <author></author>
         <link>https://padlet.com/hglenville/mv1xcs3d7j4e83ra/wish/2505820605</link>
         <description><![CDATA[<div>Inheritance pattern: sex-linked<br>&nbsp;- passed down through families through one of the X or Y chromosomes<br>- sex-linked traits usually refer to traits due to genes on the X chromosome<br>- also are disorders associated with the Y chromosome, but these are inherited less frequently because they often associate with infertility<br>- Dominant inheritance is when one parent causes the disease, even though gene from other parent is normal<br>- recessive inheritance is when both genes are abnormal<br>- many sex-linked traits are inherited in a recessive manner<br>- X-linked recessive diseases most often occur in males - a single recessive gene on that chromosome will cause disease<br>- Y chromosome doesn't contain most of the genes of the X chromosome, so doesn't protect the male<br>- females can get an X-linked recessive disorder, but it is very rare because an abnormal gene would be required from both parents<br>- if male as one abnormal gene, than disease is prevalent, if females have one abnormal gene, than they are carriers<br><br>Colour blindness:<br>- recessive gene on X chromosome<br>- males need one copy of the abnormal recessive gene to be colourblind, females need two copies to be colourblind<br>&nbsp; &nbsp; &nbsp;Symptoms:<br>- red-green colour blindness: cannot tell the difference between red and green, appear as shades of brown<br><br>Hemophilia:<br>- occurs from a recessive gene on the X chromosome<br>- affects the blood's ability to clot<br>&nbsp; &nbsp; &nbsp;Symptoms:<br>- people with hemophilia do not have as many clotting factors as they should have in their blood - they will bleed for longer than usual<br>- ie nosebleeds that take a long time to stop, bleeding gums<br><br>Duchenne Muscular Dystrophy (DMD)<br>- fatal neuromuscular disorder caused by a recessive mutation on the X chromosome<br>- DMD gene encodes dystrophin, a huge muscle protein that helps maintain structural integrity of muscle cells<br>- cells with mutated DMD genes cannot make dystrophin<br>&nbsp; &nbsp; &nbsp;Symptoms<br>- most babies do not start showing signs of disease until 3-5 years old<br>- first symptom is muscle weakness - cannot climb stairs or finds it challenging to run<br>- people often have to use a wheelchair when muscle weakness worsens<br>- often is a fatal disease when people reach 20s or 30s, results in heart or respiratory problems<br><br>Sources:<br>https://medlineplus.gov/ency/article/002051.htm#:~:text=Sex%2Dlinked%20diseases%20are%20passed,The%20abnormal%20gene%20dominates.<br>https://flexbooks.ck12.org/cbook/ck-12-middle-school-life-science-2.0/section/3.13/primary/lesson/sex-linked-inheritance-ms-ls/<br>https://www.nhs.uk/conditions/haemophilia/<br>https://www.nature.com/scitable/topicpage/sex-linked-diseases-the-case-of-duchenne-800/</div>]]></description>
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         <pubDate>2023-03-06 21:18:55 UTC</pubDate>
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         <title>Autosomal Recessive</title>
         <author></author>
         <link>https://padlet.com/hglenville/mv1xcs3d7j4e83ra/wish/2507449363</link>
         <description><![CDATA[<div>Inheritance<br>- two inherited genes that are changed or mutated (one from each parent)&nbsp;<br>- 25% unaffected, child 50% carrier (unaffected) child and 25% affected child<br>- Because the parents only have one, they are likely unaffected.&nbsp;<br>Example&nbsp;<br>- Cystic Fibrosis (CF)<br>- symptoms included: severe damage to the digestive system, lungs, and other organs in the body<br>- the cells that produce sweat, mucus, and digestive fluids are affected&nbsp;<br>- Debilitating to live with, often times they can't go to work or school </div>]]></description>
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         <pubDate>2023-03-07 19:31:41 UTC</pubDate>
         <guid>https://padlet.com/hglenville/mv1xcs3d7j4e83ra/wish/2507449363</guid>
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         <title>Autosomal Dominant </title>
         <author></author>
         <link>https://padlet.com/hglenville/mv1xcs3d7j4e83ra/wish/2508889832</link>
         <description><![CDATA[<div>Autosomal Dominant Gene Disease<br>- Abnormal Gene comes from one parent<br>- Parent with the condition has 50% chance of an affected child<br>- Abnormal gene of one of he first 22 genes&nbsp;<br>- children who do not inherit the disease will not develop or pass down the disease<br>- can occur when<br><br>HUNTINGTON'S DISEASE<br>- Causes breakdown of nerve cells in the brain<br>- main symptoms are cognitive and movement problems (muscle problems, slow eye movement, balance issues, speech difficulty, difficultly with thought process) </div>]]></description>
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         <pubDate>2023-03-08 16:36:51 UTC</pubDate>
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