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      <title>My funky padlet by Craig Weinhold</title>
      <link>https://padlet.com/craig_weinhold/2c6uok7vr5gi2vu1</link>
      <description>Made with charm</description>
      <language>en-us</language>
      <pubDate>2021-02-10 16:38:16 UTC</pubDate>
      <lastBuildDate>2021-02-10 16:48:15 UTC</lastBuildDate>
      <webMaster>hello@padlet.com</webMaster>
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         <title>Sickle Cell - Sammie R.</title>
         <author></author>
         <link>https://padlet.com/craig_weinhold/2c6uok7vr5gi2vu1/wish/1188352675</link>
         <description><![CDATA[<div>The affected gene is HBB on chromosome 11. The HBB codes for the making of a protein called Beta-globin. People with this disorder still make it, but the shape is altered. Symptoms include the C shape blood cells, pain in the spleen, liver, kidneys, lungs and heart, and the shorter lifespan of the blood cells. There are treatments including antibiotics, folic acid, and bone marrow transplant. Normal blood cells live for 120 days, sickle-shaped cells only live for 10-20 days<br><br></div>]]></description>
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         <pubDate>2021-02-10 16:39:27 UTC</pubDate>
         <guid>https://padlet.com/craig_weinhold/2c6uok7vr5gi2vu1/wish/1188352675</guid>
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      <item>
         <title>Cystic Fibrosis- Conrad</title>
         <author></author>
         <link>https://padlet.com/craig_weinhold/2c6uok7vr5gi2vu1/wish/1188352752</link>
         <description><![CDATA[<div>1.You inherit cystic fibrosis by having a copy the cystic fibrosis trans membrane from each parent. <br><br>2.Some symptoms of CF are a cough, shortness of breath, delayed development and heartburn. <br><br>3.No, there is no cure to CF, but you can use treatments. </div>]]></description>
         <enclosure url="" />
         <pubDate>2021-02-10 16:39:28 UTC</pubDate>
         <guid>https://padlet.com/craig_weinhold/2c6uok7vr5gi2vu1/wish/1188352752</guid>
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      <item>
         <title>Sickle Cell-Amy</title>
         <author></author>
         <link>https://padlet.com/craig_weinhold/2c6uok7vr5gi2vu1/wish/1188353113</link>
         <description><![CDATA[<div>Sickle cell disease is an inherited blood disorder marked by defective hemoglobin. It inhibits the ability of hemoglobin in red blood cells to carry oxygen. <br><br>The affected gene in sickle cell disease is HBB, on chromosome 11. The HBB gene codes for a protein called beta-globin.<br><br>-Stiff, pointy red blood cells can get caught in small blood vessels which cause pain and damage organs. The spleen is often affected, along with the liver, kidneys, lungs, and heart. When the spleen is damaged, the body is less able to fight infections.<br><br>This condition is <strong>inherited</strong> in an autosomal recessive pattern , which means both copies of the gene in each <strong>cell</strong> have mutations.<br><br>The only treatment that can offer a potential cure for sickle cell disease is stem cell transplantation. </div>]]></description>
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         <pubDate>2021-02-10 16:39:32 UTC</pubDate>
         <guid>https://padlet.com/craig_weinhold/2c6uok7vr5gi2vu1/wish/1188353113</guid>
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         <title>Galactosemia - Gisselle</title>
         <author></author>
         <link>https://padlet.com/craig_weinhold/2c6uok7vr5gi2vu1/wish/1188353614</link>
         <description><![CDATA[<div>People are unable to breakdown a type of sugar found in milk or any other dairy product. With that it can harm body tissue's. <br>- people with this have two non-working copies of GALT gene <br>Treatment:<br>managed through nutrition <br><br><br></div>]]></description>
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         <pubDate>2021-02-10 16:39:36 UTC</pubDate>
         <guid>https://padlet.com/craig_weinhold/2c6uok7vr5gi2vu1/wish/1188353614</guid>
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         <title>neurofribromatosis type 1 (NF1)- Kendall</title>
         <author></author>
         <link>https://padlet.com/craig_weinhold/2c6uok7vr5gi2vu1/wish/1188353725</link>
         <description><![CDATA[<div>The affected gene, also called NF1, codes for a protein called neurofibromin. People with NF-1 have an altered form of the gene, and so they make a form of the protein that does not do its job.<br>The symptoms include non-cancerous tumors, scoliosis, café au lait spots (coffee with milk colored spots), bone defects, vision and hearing loss.<br>1 in every 3,000 people have this disease<br>there is no cure </div>]]></description>
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         <pubDate>2021-02-10 16:39:37 UTC</pubDate>
         <guid>https://padlet.com/craig_weinhold/2c6uok7vr5gi2vu1/wish/1188353725</guid>
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         <title>Galactosemia- Naydelin G</title>
         <author></author>
         <link>https://padlet.com/craig_weinhold/2c6uok7vr5gi2vu1/wish/1188354116</link>
         <description><![CDATA[<div>Is type of disease that does not have the system to be able to break down sugar, milk anything that is daily products.<br>The symptoms to have this disease takes days to noticed if they have it. when babys start drinking breast milk or the formula, later once it dosent work they start to vomit. </div>]]></description>
         <enclosure url="" />
         <pubDate>2021-02-10 16:39:41 UTC</pubDate>
         <guid>https://padlet.com/craig_weinhold/2c6uok7vr5gi2vu1/wish/1188354116</guid>
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      <item>
         <title>Sickle cell </title>
         <author>dtpeterson01</author>
         <link>https://padlet.com/craig_weinhold/2c6uok7vr5gi2vu1/wish/1188354262</link>
         <description><![CDATA[<div>is a genetic disease that causes blood cells to not be circle but in curved sickle shapes this is not good at is can clog up the blood flow and oxygen flow in the body </div>]]></description>
         <enclosure url="" />
         <pubDate>2021-02-10 16:39:43 UTC</pubDate>
         <guid>https://padlet.com/craig_weinhold/2c6uok7vr5gi2vu1/wish/1188354262</guid>
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         <title>Theo - MSUD</title>
         <author></author>
         <link>https://padlet.com/craig_weinhold/2c6uok7vr5gi2vu1/wish/1188354970</link>
         <description><![CDATA[<div>MSUD is a rare genetic disorder which causes people to not be able to break down 3 amino acids. The affected gene is BCKHDA, but can also be BCKHDB or DBT. MSUD is managed by a diet, usually avoiding high protein foods.</div>]]></description>
         <enclosure url="" />
         <pubDate>2021-02-10 16:39:50 UTC</pubDate>
         <guid>https://padlet.com/craig_weinhold/2c6uok7vr5gi2vu1/wish/1188354970</guid>
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         <title>Sickle cell disease- Luis Mario Aguilar</title>
         <author>lmaguilar01</author>
         <link>https://padlet.com/craig_weinhold/2c6uok7vr5gi2vu1/wish/1188355207</link>
         <description><![CDATA[<div>1. One of the parents or the both of them have a mutated sickle cell disease but do not show symptoms which is how it gets to the offspring.<br><br>2. symptoms:<br>- Anemia. Sickle cells break apart easily and die, leaving you with too few red blood cells. </div><ul><li>Episodes of pain. Periodic episodes of pain, called pain crisis, are a major symptom of sickle cell anemia. ...</li><li>Swelling of hands and feet.</li><li>Frequent infection . ...</li><li>Delayed growth or puberty.</li><li>Vision problems</li></ul><div><br>3. The only known cure of sickle cell disease is bone marrow or stem cell transplant.</div>]]></description>
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         <pubDate>2021-02-10 16:39:52 UTC</pubDate>
         <guid>https://padlet.com/craig_weinhold/2c6uok7vr5gi2vu1/wish/1188355207</guid>
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      <item>
         <title>Galactosemia - Ava Cabanillas</title>
         <author></author>
         <link>https://padlet.com/craig_weinhold/2c6uok7vr5gi2vu1/wish/1188355356</link>
         <description><![CDATA[<div>People with galactosemia are unable to break down galactose, a type of sugar found in milk and other dairy products. The most commonly affected gene is GALT. GALT protein breaks down the sugar galactose. Galactosemia is managed through diet. Babies receive a galactose-free formula. Children with the disorder must stay away from foods and drinks containing galactose. These foods include milk, cheese, and legumes.</div>]]></description>
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         <pubDate>2021-02-10 16:39:53 UTC</pubDate>
         <guid>https://padlet.com/craig_weinhold/2c6uok7vr5gi2vu1/wish/1188355356</guid>
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      <item>
         <title>Phenylketonuria - Davis</title>
         <author></author>
         <link>https://padlet.com/craig_weinhold/2c6uok7vr5gi2vu1/wish/1188356218</link>
         <description><![CDATA[<div>Usually, each parent of an individual who has PKU carries one copy of the altered gene.A musty odor in the breath, skin or urine, caused by too much phenylalanine in the body. Neurological problems that may include seizures. Skin rashes (eczema) Fair skin and blue eyes, because phenylalanine can't transform into melanin — the pigment responsible for hair and skin tone.There is no cure for PKU, but treatment can prevent intellectual disabilities and other health problems. A person with PKU should receive treatment at a medical center that specializes in the disorder.</div>]]></description>
         <enclosure url="" />
         <pubDate>2021-02-10 16:40:02 UTC</pubDate>
         <guid>https://padlet.com/craig_weinhold/2c6uok7vr5gi2vu1/wish/1188356218</guid>
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      <item>
         <title>Annabelle - Huntington&#39;s Disease</title>
         <author>agworam01</author>
         <link>https://padlet.com/craig_weinhold/2c6uok7vr5gi2vu1/wish/1188357610</link>
         <description><![CDATA[<div>Huntington's disease is caused by a single defective gene on chromosome 4. Huntington's disease causes neurons in parts of the brain to gradually break down and die. This disease gets worse over time and attacks the motor control regions of the brain as well as other areas.</div>]]></description>
         <enclosure url="" />
         <pubDate>2021-02-10 16:40:16 UTC</pubDate>
         <guid>https://padlet.com/craig_weinhold/2c6uok7vr5gi2vu1/wish/1188357610</guid>
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      <item>
         <title>MSUD - Alan</title>
         <author></author>
         <link>https://padlet.com/craig_weinhold/2c6uok7vr5gi2vu1/wish/1188364675</link>
         <description><![CDATA[<div>Maple syrup urine disease is </div>]]></description>
         <enclosure url="" />
         <pubDate>2021-02-10 16:41:16 UTC</pubDate>
         <guid>https://padlet.com/craig_weinhold/2c6uok7vr5gi2vu1/wish/1188364675</guid>
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      <item>
         <title>Maple Syrup Urine Disease - Eliot Nance</title>
         <author></author>
         <link>https://padlet.com/craig_weinhold/2c6uok7vr5gi2vu1/wish/1188365543</link>
         <description><![CDATA[<div>People with MSUD cannot break down three amino acids: leucine, isoleucine, and valine. These amino acids come from protein in food; they are released into the blood stream during digestion. Our cells can either recycle them by adding them to new proteins, or break them down for energy. If they are not used or broken down, they can build up to levels that are harmful to the body.</div>]]></description>
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         <pubDate>2021-02-10 16:41:20 UTC</pubDate>
         <guid>https://padlet.com/craig_weinhold/2c6uok7vr5gi2vu1/wish/1188365543</guid>
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      <item>
         <title>Factor V Leiden</title>
         <author></author>
         <link>https://padlet.com/craig_weinhold/2c6uok7vr5gi2vu1/wish/1188382680</link>
         <description><![CDATA[<div>An inherited blood-clotting disorder due to a mutation of the blood's factor V protein. Factor V Leiden  increases the chance of clumps of blood clots developing, which can be life threatening. Women with the disorder risk developing blood clots during pregnancy of while taking the hormone estrogen.</div>]]></description>
         <enclosure url="" />
         <pubDate>2021-02-10 16:44:10 UTC</pubDate>
         <guid>https://padlet.com/craig_weinhold/2c6uok7vr5gi2vu1/wish/1188382680</guid>
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