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      <title>My Bone disease Research by Curtrell Rhodan</title>
      <link>https://padlet.com/crhodan1/w5iu0rlzlqrskcxc</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 13:27:05 UTC</pubDate>
      <lastBuildDate>2021-01-12 14:07:07 UTC</lastBuildDate>
      <webMaster>hello@padlet.com</webMaster>
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      <item>
         <title>Sylve </title>
         <author></author>
         <link>https://padlet.com/crhodan1/w5iu0rlzlqrskcxc/wish/1078383292</link>
         <description><![CDATA[<div><br>1. <strong>Marfan Syndrome </strong><br>A mutation or change in the fibrillin-1 (FBN1) gene causes Marfan syndrome.<br> 2. <strong>Osteogenesis Imperfecta</strong><br>A mutation or change in a gene causes OI.<br>3. <strong>Bursitis</strong><br>is usually caused by overusing a joint or trauma to a joint.<br>4. <strong>Osteopetrosis</strong></div><div>is a genetic disease that, in most cases, a child inherits from one or both parents.<br>5. <strong>Fibrous</strong><br>Fibrous dysplasia happens when a gene mutates after conception, early in the pregnancy</div><div><br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2021-01-12 13:29:32 UTC</pubDate>
         <guid>https://padlet.com/crhodan1/w5iu0rlzlqrskcxc/wish/1078383292</guid>
      </item>
      <item>
         <title>Teriyonah</title>
         <author></author>
         <link>https://padlet.com/crhodan1/w5iu0rlzlqrskcxc/wish/1078383891</link>
         <description><![CDATA[<div>1. Enchondroma- The cell turn into cartilage and not a bone. <br>2. Osteoid Osteoma- Cells divide uncontrollably, forming a small mass of bone and other tissue. <br>3.Bone Spurs- Joint damage from osteoarthritis <br>4.Fibrous Dysplasia-gene changes after conception<br>5. Hypophophatasia-low levels of an enzyme called ALP<br>Findings-https://orthoinfo.aaos.org/en/diseases--conditions, <strong>https://www.mayoclinic.org/diseases-conditions</strong><br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2021-01-12 13:29:41 UTC</pubDate>
         <guid>https://padlet.com/crhodan1/w5iu0rlzlqrskcxc/wish/1078383891</guid>
      </item>
      <item>
         <title>Asia </title>
         <author></author>
         <link>https://padlet.com/crhodan1/w5iu0rlzlqrskcxc/wish/1078385519</link>
         <description><![CDATA[<div>1. Chondroblastoma- Inquiry, Rare type of benign tumor that grows at the end of long bones and closed joints.They are found close to the knee joint, thighbone, and shinbone.<br>2. <mark>Hypophosphatasia-</mark>Inherited, Bone disease that results from low levels of an enzyme called phosphatase.<br>3. <mark>Diastrofic Dysplasia</mark>- Genetic, caused by mutations in the gene that alters the structure of developing cartilage, preventing bones from forming properly, and resulting in skeletal problems. <br>4. <mark>Miller syndrome</mark>- Genetic, affects the development of the faces and limbs<br>5. Pyle Disease- Genetic, The ends of long bones in the arms and legs are the shape of a boat oar or paddle<br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2021-01-12 13:30:06 UTC</pubDate>
         <guid>https://padlet.com/crhodan1/w5iu0rlzlqrskcxc/wish/1078385519</guid>
      </item>
      <item>
         <title>Grace</title>
         <author></author>
         <link>https://padlet.com/crhodan1/w5iu0rlzlqrskcxc/wish/1078387481</link>
         <description><![CDATA[<div>1. Fibrous Dysplasia- Genetic<br>2. Adams-Olivers Syndrome- Genetic<br>3. Platyspondylic Lethal Skeletal Dysplasia- Genetic<br>4. Osteomyelitis- Infectious<br>5. Osteoarthritis- Genetic<br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2021-01-12 13:30:38 UTC</pubDate>
         <guid>https://padlet.com/crhodan1/w5iu0rlzlqrskcxc/wish/1078387481</guid>
      </item>
      <item>
         <title>Hayden Scudder</title>
         <author></author>
         <link>https://padlet.com/crhodan1/w5iu0rlzlqrskcxc/wish/1078387552</link>
         <description><![CDATA[<div>1. Bone tumor<br>2. Osteoporosis<br>3. Fibrous Dysplasia <br>4.   Hypophosphatasia <br>5. Winchester syndrome </div>]]></description>
         <enclosure url="" />
         <pubDate>2021-01-12 13:30:39 UTC</pubDate>
         <guid>https://padlet.com/crhodan1/w5iu0rlzlqrskcxc/wish/1078387552</guid>
      </item>
      <item>
         <title>Ejuan Jones </title>
         <author></author>
         <link>https://padlet.com/crhodan1/w5iu0rlzlqrskcxc/wish/1078389324</link>
         <description><![CDATA[<div>1. Campomelic dysplasia<br>2. Otopalatodigital syndrome type 2, genetic <br>3. Nager syndrome- genetic<br>4. Klippel-Feil Syndrome <br>5. Bone Spurs</div>]]></description>
         <enclosure url="" />
         <pubDate>2021-01-12 13:31:05 UTC</pubDate>
         <guid>https://padlet.com/crhodan1/w5iu0rlzlqrskcxc/wish/1078389324</guid>
      </item>
      <item>
         <title>Da&#39;Corin Johnson</title>
         <author>1188319</author>
         <link>https://padlet.com/crhodan1/w5iu0rlzlqrskcxc/wish/1078391697</link>
         <description><![CDATA[<h1>1.Stüve-Wiedemann syndrome-Lifr gene</h1><div>2.Osteochondroma-  Associated with EXT 1 gene</div><h1>3,Klippel-Feil syndrome- Mutation in the GDF6, GDF3, MEO1 gene</h1><h1>4.Hereditary multiple osteochondromas- genetic</h1><h1>5. Langer mesomelic dysplasia- genectic</h1><div><a href="mailto:?subject=Langer%20mesomelic%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%2Flanger-mesomelic-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><div><a href="mailto:?subject=Hereditary%20multiple%20osteochondromas%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%2Fhereditary-multiple-osteochondromas%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><div><br></div><div><a href="mailto:?subject=St%C3%BCve-Wiedemann%20syndrome%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%2Fstuve-wiedemann-syndrome%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><div><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2021-01-12 13:31:42 UTC</pubDate>
         <guid>https://padlet.com/crhodan1/w5iu0rlzlqrskcxc/wish/1078391697</guid>
      </item>
      <item>
         <title>LaJaden Fleming </title>
         <author></author>
         <link>https://padlet.com/crhodan1/w5iu0rlzlqrskcxc/wish/1078394920</link>
         <description><![CDATA[<div>1. Caffey disease (genetic)<br>2. Melnick-Needles syndrome (genetic)<br>3. Proteus syndrome (genetic)<br>4. Osteoid Osteoma (unknown)<br>5. Osteochondritis dissecans (unknown)</div>]]></description>
         <enclosure url="" />
         <pubDate>2021-01-12 13:32:33 UTC</pubDate>
         <guid>https://padlet.com/crhodan1/w5iu0rlzlqrskcxc/wish/1078394920</guid>
      </item>
      <item>
         <title>Ash </title>
         <author></author>
         <link>https://padlet.com/crhodan1/w5iu0rlzlqrskcxc/wish/1078398247</link>
         <description><![CDATA[<div>I. Osteoporosis: <strong> </strong>a decrease in the density of bones weakens the bones, making breaks (fractures) likely. (?)<br>II. Osteochondroma: Unknown, but thought to be associated with the EXT 1 gene.<br>III. Klippel-Feil Syndrome: a failure in the normal segmentation or division of the cervical vertebrae during the early weeks of fetal development.<br>IV. Fibrous Dysplasia: when a gene mutates while the baby is developing in the womb. The changes in the gene cause bone-forming cells to fail to mature.<br>V. Osteoid Osteoma: Unknown, unfortunately</div>]]></description>
         <enclosure url="" />
         <pubDate>2021-01-12 13:33:24 UTC</pubDate>
         <guid>https://padlet.com/crhodan1/w5iu0rlzlqrskcxc/wish/1078398247</guid>
      </item>
      <item>
         <title>Peyton</title>
         <author></author>
         <link>https://padlet.com/crhodan1/w5iu0rlzlqrskcxc/wish/1078401701</link>
         <description><![CDATA[<div>1.Blount Disease (unknown)<br>2.Hyperparathyroidism (Growth or Radiation to your head or thyroid)<br>3.Fibrous Dysplasia (genetic)<br>4.Fibrochondrogenesis (Mutations involved with a gene in your body)<br>5.Osteoporosis (age or anything to weaken the bones, genetics)</div>]]></description>
         <enclosure url="" />
         <pubDate>2021-01-12 13:34:12 UTC</pubDate>
         <guid>https://padlet.com/crhodan1/w5iu0rlzlqrskcxc/wish/1078401701</guid>
      </item>
      <item>
         <title>Dante Burton</title>
         <author>020572</author>
         <link>https://padlet.com/crhodan1/w5iu0rlzlqrskcxc/wish/1078402075</link>
         <description><![CDATA[<div>1.Boomerang dysplasia - Genetic <br>2. osteomyelitis - Bacterial Infection<br>3. Fibrous Dysplasia- Genetic<br>4. Osteoporosis-Genetic<br>5.Nager syndrome- Genetic</div>]]></description>
         <enclosure url="" />
         <pubDate>2021-01-12 13:34:16 UTC</pubDate>
         <guid>https://padlet.com/crhodan1/w5iu0rlzlqrskcxc/wish/1078402075</guid>
      </item>
      <item>
         <title>Chloe Williams</title>
         <author></author>
         <link>https://padlet.com/crhodan1/w5iu0rlzlqrskcxc/wish/1078403001</link>
         <description><![CDATA[<div>1.Osteogenesis - defective genes; specifically the genes responsible for making collagen<br>2. Skeletal Dysplasia-  defective genes<br>3. Osteonecrosis- Alcohol use, corticosteroid use, or history of trauma<br>4. Paget's Disease of Bone- Age/runs in the family <br>5. Scoliosis- Cerebral palsy, muscular dystrophy, but most causes are idiopathic ( no known origin )</div>]]></description>
         <enclosure url="" />
         <pubDate>2021-01-12 13:34:29 UTC</pubDate>
         <guid>https://padlet.com/crhodan1/w5iu0rlzlqrskcxc/wish/1078403001</guid>
      </item>
      <item>
         <title>Kierra</title>
         <author></author>
         <link>https://padlet.com/crhodan1/w5iu0rlzlqrskcxc/wish/1078410696</link>
         <description><![CDATA[<div>1. Osteomyelitis- infectious- inflammation of the bone <br>2. Melorheostosis- genetic- abnormal growth of bones <br>3. Achondroplasia- genetic- short-limbed dwarfism <br>4. Osteoporosis- genetic- makes bones weak<br>5. Osteogenesis- genetic- brittle bone disease</div>]]></description>
         <enclosure url="" />
         <pubDate>2021-01-12 13:36:20 UTC</pubDate>
         <guid>https://padlet.com/crhodan1/w5iu0rlzlqrskcxc/wish/1078410696</guid>
      </item>
      <item>
         <title>Lindsey</title>
         <author>023486</author>
         <link>https://padlet.com/crhodan1/w5iu0rlzlqrskcxc/wish/1078417505</link>
         <description><![CDATA[<div>1. Bone Spurs: usually acquired from joint damage from osteoarthritis<br>2. Hypophosphatasia: an inherited bone disease where the body has low levels of the enzyme alkaline phosphatase <br>3. Osteopetrosis: genetic abnormality in certain genes that cause body not to recycle old bone cells<br>4. Diastrophic Displaysia: inherited in an autosomal recessive pattern<br>5. Miller syndrome: gene mutations</div>]]></description>
         <enclosure url="" />
         <pubDate>2021-01-12 13:37:58 UTC</pubDate>
         <guid>https://padlet.com/crhodan1/w5iu0rlzlqrskcxc/wish/1078417505</guid>
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