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      <title>8b My Bone disease Research by Curtrell Rhodan</title>
      <link>https://padlet.com/crhodan1/rgd6bsad7ax2llau</link>
      <description>Use the websites given in the chat and quickly research 5 diseases and their main cause. Put your findings in the chat</description>
      <language>en-us</language>
      <pubDate>2021-01-12 20:21:05 UTC</pubDate>
      <lastBuildDate>2021-01-19 13:18:43 UTC</lastBuildDate>
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         <title>Alaina</title>
         <author></author>
         <link>https://padlet.com/crhodan1/rgd6bsad7ax2llau/wish/1080577974</link>
         <description><![CDATA[<div>rickets: A softening and weakening of bones in children, usually due to inadequate vitamin D, makes their legs extremely boe legged. osteoporosis, <a href="https://vsearch.nlm.nih.gov/vivisimo/cgi-bin/query-meta?v%3afile=viv_4qArGH&amp;server=pvlb7srch11&amp;v%3astate=root%7croot&amp;url=https%3a%2f%2fmedlineplus.gov%2fosteogenesisimperfecta.html&amp;rid=Ndoc2&amp;v%3aframe=redirect&amp;v%3aredirect-hash=cd5c6d5ab1a21613fb34bbb339869891&amp;">Osteogenesis Imperfecta</a>, </div>]]></description>
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         <pubDate>2021-01-12 20:22:02 UTC</pubDate>
         <guid>https://padlet.com/crhodan1/rgd6bsad7ax2llau/wish/1080577974</guid>
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         <title>Brandon</title>
         <author></author>
         <link>https://padlet.com/crhodan1/rgd6bsad7ax2llau/wish/1080578276</link>
         <description><![CDATA[<h1>1. Ghosal hematodiaphyseal dysplasia (Genetic)</h1><div>2. Greenberg dysplasia (Genetic)<br>3. </div><div><a href="mailto:?subject=Greenberg%20dysplasia%3A%20MedlinePlus%20Genetics&amp;body=I%20found%20this%20information%20on%20MedlinePlus.gov%20and%20I%27d%20like%20to%20share%20it%20with%20you%3A%0A%0Ahttps%3A%2F%2Fmedlineplus.gov%2Fgenetics%2Fcondition%2Fgreenberg-dysplasia%2F%3Futm_source%3Demail%26utm_medium%3Dshare%26utm_campaign%3Dmplus_share%0A%0AMedlinePlus%20(https%3A%2F%2Fmedlineplus.gov)%3A%20Trusted%20Health%20Information%20for%20you%0A%0ATo%20get%20updates%20by%20email%20when%20new%20information%20becomes%20available%20on%20MedlinePlus%2C%20sign%20up%20at%20https%3A%2F%2Fmedlineplus.gov%2Flistserv.html."><br></a><br></div>]]></description>
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         <pubDate>2021-01-12 20:22:07 UTC</pubDate>
         <guid>https://padlet.com/crhodan1/rgd6bsad7ax2llau/wish/1080578276</guid>
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         <title>Zy</title>
         <author></author>
         <link>https://padlet.com/crhodan1/rgd6bsad7ax2llau/wish/1080578343</link>
         <description><![CDATA[<div>Bone Spurs-Joint damage from osteoarthritis <br>Fibrous Dysplasia-gene mutastes afer conception<br>Enchondroma-Unknown cause <br><br><br></div>]]></description>
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         <pubDate>2021-01-12 20:22:08 UTC</pubDate>
         <guid>https://padlet.com/crhodan1/rgd6bsad7ax2llau/wish/1080578343</guid>
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      <item>
         <title>Shayla </title>
         <author></author>
         <link>https://padlet.com/crhodan1/rgd6bsad7ax2llau/wish/1080579550</link>
         <description><![CDATA[<div>1. Osteoporosis: Common bone disease that causes the bone to become brittle and weak. Exact cause is unknown ,but things like being a women and not getting enough calcium increase your risk.<br>2. Scoliosis: An abnormal curve at the spine. It can be caused by malformed vertebrae (born with it)  or the cause can be unknown. (develops during growth spur) <br>3. Gout: Sudden joint pain. Cause by uric acid build up. <br>4.Melnick-Needle Syndrome: Abnormal skeletal development. It is genetic.<br>5. Bone spur: Bony projections along edges. Cause by joint damage.</div>]]></description>
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         <pubDate>2021-01-12 20:22:27 UTC</pubDate>
         <guid>https://padlet.com/crhodan1/rgd6bsad7ax2llau/wish/1080579550</guid>
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      <item>
         <title>Fabiana</title>
         <author></author>
         <link>https://padlet.com/crhodan1/rgd6bsad7ax2llau/wish/1080579809</link>
         <description><![CDATA[<div>1. caffey disease- is caused by a mutation in the COL1A1 gene<br>2.  miller syndrome- is caused by mutation in the dihydroorotate dehydrogenase<br>3. Fibrous dysplasia- is not know <br>4. cantu syndrome- results from mutations in the ABCC9 gene.<br>5. diastrophic dysplasia- is caused by an autosomal recessive disorder on the gene called DTDST</div>]]></description>
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         <pubDate>2021-01-12 20:22:31 UTC</pubDate>
         <guid>https://padlet.com/crhodan1/rgd6bsad7ax2llau/wish/1080579809</guid>
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         <title>Shelby</title>
         <author></author>
         <link>https://padlet.com/crhodan1/rgd6bsad7ax2llau/wish/1080580098</link>
         <description><![CDATA[<div>1. Chondroblastoma- believed to start from immature cartilage producing cells called chondroblasts<br>2.Bone spurs - joint damage from osteoarthritis<br>3.Osteoporosis- lifelong lack of calcium, eating disorders<br>4.bone tumor- genetics, radiation treatment, broken bones<br><br></div>]]></description>
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         <pubDate>2021-01-12 20:22:35 UTC</pubDate>
         <guid>https://padlet.com/crhodan1/rgd6bsad7ax2llau/wish/1080580098</guid>
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      <item>
         <title>Chloe</title>
         <author></author>
         <link>https://padlet.com/crhodan1/rgd6bsad7ax2llau/wish/1080581817</link>
         <description><![CDATA[<div>1) Campomelic Dysplasia: inherited in an autosomal dominant pattern, meaning that 1 gene in each cell is sufficient to cause the disorder but people have no history of the disorder in the family<br>2) Winchester Syndrome: a rare inherited disease characterized by a loss of bone tissue<br>3)Tarsal-carpal coalition syndrome: a rare, inherited bone disorder that affects primarily the hands and feet<br>4)Acromicric Dysplasia: caused by mutations in the FBN1 gene, which provides instructions for making a large protein called fibrillin-1.<br>5)Boomerang Dysplasia: a disorder that affects the development of bones throughout the body. Mutations in the F<em>LNB</em> gene cause boomerang dysplasia</div>]]></description>
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         <pubDate>2021-01-12 20:23:04 UTC</pubDate>
         <guid>https://padlet.com/crhodan1/rgd6bsad7ax2llau/wish/1080581817</guid>
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      <item>
         <title>emily</title>
         <author></author>
         <link>https://padlet.com/crhodan1/rgd6bsad7ax2llau/wish/1080582499</link>
         <description><![CDATA[<div>1) Extra-Abdominal Desmoid Tumors- is not known.<br>2) bone spurs- Joint damage from osteoarthritis<br>3) Hypophosphatasia- <strong>caused</strong> by mutations in the tissue nonspecific alkaline phosphatase gene<br>4)Osteochondritis dissecans- a loss of blood supply to the area<br>5)Chondroblastoma- is not known</div>]]></description>
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         <pubDate>2021-01-12 20:23:14 UTC</pubDate>
         <guid>https://padlet.com/crhodan1/rgd6bsad7ax2llau/wish/1080582499</guid>
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      <item>
         <title>Dorothy</title>
         <author></author>
         <link>https://padlet.com/crhodan1/rgd6bsad7ax2llau/wish/1080588186</link>
         <description><![CDATA[<div>1.bone tumor-cells within a bone divide uncontrollably, forming a lump or mass of abnormal tissue.<br>2.fibrous Dysplasia-abnormal fibrous (scar-like) tissue replaces healthy bone.<br>3.enchondroma- tumor that begins in the cartilage found inside the bones. <br><br></div>]]></description>
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         <pubDate>2021-01-12 20:24:28 UTC</pubDate>
         <guid>https://padlet.com/crhodan1/rgd6bsad7ax2llau/wish/1080588186</guid>
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      <item>
         <title> Cantu Syndrome- , Larsen Syndrome, Juvenile Paget, Majeed Syndrome, Miller Syndrome</title>
         <author></author>
         <link>https://padlet.com/crhodan1/rgd6bsad7ax2llau/wish/1080595895</link>
         <description><![CDATA[<div>Sianni<br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2021-01-12 20:26:13 UTC</pubDate>
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