<?xml version="1.0" encoding="UTF-8"?>
<communities type="array">
  <community>
    <causes></causes>
    <created-at type="datetime">2008-05-21T13:25:32+00:00</created-at>
    <description>&lt;p&gt;Radiation Proctitis is inflammation and damage to the lower parts of the colon after exposure to x-rays or other ionizing radiation as a part of radiation therapy.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Radiation Proctitis is inflammation and damage to the lower parts of the colon after exposure to x-rays or other ionizing radiation as a part of radiation therapy.&lt;/p&gt;</disorder-description>
    <expert-id type="integer" nil="true"></expert-id>
    <general-symptoms></general-symptoms>
    <general-test></general-test>
    <general-treatment></general-treatment>
    <id type="integer">541</id>
    <name>Radiation Proctitis</name>
    <participations-count type="integer">1</participations-count>
    <permalink>radiation-proctitis</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal">35.0</prevalence-number>
    <prevalence-number-source-url>http://www.orpha.net</prevalence-number-source-url>
    <prevalence-type>Per 100,000 Population</prevalence-type>
    <prognosis></prognosis>
    <symptoms-count type="integer" nil="true"></symptoms-count>
    <synonym-tags></synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2009-10-20T14:42:04+00:00</updated-at>
  </community>
  <community>
    <causes></causes>
    <created-at type="datetime">2009-09-17T15:20:23+00:00</created-at>
    <description>&lt;p&gt;Radioulnar Synostosis is the abnormal development of the radio-ulnar joint.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Radioulnar Synostosis is the abnormal development of the radio-ulnar joint. In this rare condition there is congenital fusion of the proximal ends of the radius and ulna, which severely restricts supination of the forearm and, consequently, puts unusual strain on the elbow and shoulder. In about 60 percent of cases, involvement is bilateral.&lt;/p&gt;</disorder-description>
    <expert-id type="integer" nil="true"></expert-id>
    <general-symptoms>&lt;p&gt;Severely restricted supination means that one cannot take change &amp;#8212; the palm cannot be made flat, so the coins fall. It is impossible to touch the shoulders with the thumbs or to hold silverware the way other people do. It is also impossible to play bar chords on a guitar or throw a football properly. Club foot often occurs with this genetic anomaly and sufferers should be checked for heart and kidney problems.&lt;/p&gt;</general-symptoms>
    <general-test></general-test>
    <general-treatment>&lt;p&gt;Surgical intervention is possible but rarely successful. The bones usually re-fuse and the best that can generally be done is to reset the arms so that when the bones fuse back together the neutral position is more supinated. Blood supply in the arm is often jeopardized by surgery.&lt;/p&gt;</general-treatment>
    <id type="integer">1437</id>
    <name>Radioulnar Synostosis</name>
    <participations-count type="integer">2</participations-count>
    <permalink>radioulnar-synostosis</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal" nil="true"></prevalence-number>
    <prevalence-number-source-url></prevalence-number-source-url>
    <prevalence-type>Per 100,000 Population</prevalence-type>
    <prognosis>&lt;p&gt;See these websites:&lt;/p&gt;
&lt;p&gt;http://boneandspine.com/pediatric-disorders/congenital-radioulnar-synostosis/&lt;/p&gt;
&lt;p&gt;http://www.arbi.org/prevention/conanomi.html&lt;/p&gt;
&lt;p&gt;http://ehealthforum.com/health/radioulnar-synostosis-t161296.html&lt;/p&gt;
&lt;p&gt;http://www.righthealth.com/topic/Radioulnar_Synostosis&lt;/p&gt;
&lt;p&gt;http://rarediseases.info.nih.gov/&lt;span class="caps"&gt;GARD&lt;/span&gt;/Condition/4630/Radioulnar_synostosis_type_1.aspx&lt;/p&gt;
&lt;p&gt;http://emedicine.medscape.com/article/1240467-overview&lt;/p&gt;</prognosis>
    <symptoms-count type="integer" nil="true"></symptoms-count>
    <synonym-tags>Radio-Ulnar Synostosis, Radio Ulnar Synostosis</synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">1</topics-count>
    <updated-at type="datetime">2009-12-13T02:43:02+00:00</updated-at>
  </community>
  <community>
    <causes></causes>
    <created-at type="datetime">2009-04-22T17:37:29+00:00</created-at>
    <description>&lt;p&gt;Ramsay Hunt Syndrome Type 2 results from nerve damage caused by shingles in the ear, causing facial paralysis and damage to the 7th cranial nerve causing severe headaches.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Ramsay Hunt Syndrome Type 2 results from nerve damage caused by shingles in the ear, causing facial paralysis and damage to the 7th cranial nerve causing severe headaches.&lt;/p&gt;</disorder-description>
    <expert-id type="integer" nil="true"></expert-id>
    <general-symptoms></general-symptoms>
    <general-test></general-test>
    <general-treatment></general-treatment>
    <id type="integer">1378</id>
    <name>Ramsay Hunt Syndrome Type 2</name>
    <participations-count type="integer">1</participations-count>
    <permalink>ramsay-hunt-syndrome-type-2</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal" nil="true"></prevalence-number>
    <prevalence-number-source-url></prevalence-number-source-url>
    <prevalence-type>Per 100,000 Population</prevalence-type>
    <prognosis></prognosis>
    <symptoms-count type="integer" nil="true"></symptoms-count>
    <synonym-tags>Ramsay Hunt Syndrome Type II, RHS Type II, RHS Type 2</synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2009-04-22T17:37:29+00:00</updated-at>
  </community>
  <community>
    <causes>&lt;p&gt;No known causes at this time.&lt;/p&gt;</causes>
    <created-at type="datetime">2009-01-04T18:53:43+00:00</created-at>
    <description>&lt;p&gt;&lt;span class="caps"&gt;ROHHAD&lt;/span&gt; Syndrome (Rapid-onset Obesity with Hypothalamic dysfunction, Hypoventilation and Autonomic Dysregulation) is a rare disorder in which affects the governace of proper breathing.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Rapid-onset Obesity with Hypothalamic dysfunction, Hypoventilation and Autonomic Dysregulation (&lt;span class="caps"&gt;ROHHAD&lt;/span&gt; syndrome) is a very rare disease affecting approximately only 35 cases worldwide.&lt;/p&gt;
&lt;p&gt;Patients with &lt;span class="caps"&gt;ROHHAD&lt;/span&gt;,as well as patients with Congenital Central Hypoventilation Syndrome, &lt;span class="caps"&gt;CCHS&lt;/span&gt;, have damaged the mechanism governing the proper breathing. &lt;span class="caps"&gt;ROHHAD&lt;/span&gt; syndrome is a disease that is potentially lethal and incurable.&lt;/p&gt;</disorder-description>
    <expert-id type="integer" nil="true"></expert-id>
    <general-symptoms>&lt;p&gt;Hypothalamic Dysfunction &lt;br /&gt;
Failed Growth Hormone Stimulation &lt;br /&gt;
Polydipsia &lt;br /&gt;
Hypernatremia &lt;br /&gt;
Hyperprolactinemia &lt;br /&gt;
Hyperphagia &lt;br /&gt;
Diabetes Insipidus&lt;/p&gt;
&lt;p&gt;Respiratory Manifestations &lt;br /&gt;
Alveolar Hypoventilation &lt;br /&gt;
Cardiorespiratory Arrest &lt;br /&gt;
Reduced Carbon Dioxide Ventilatory Response &lt;br /&gt;
Obstructive sleep apnea&lt;/p&gt;
&lt;p&gt;Autonomic Dysregulation &lt;br /&gt;
Ophthalmologic Manifestations &lt;br /&gt;
Thermal Dysregulation &lt;br /&gt;
Gastrointestinal Dysmotility &lt;br /&gt;
Altered Perception of Pain &lt;br /&gt;
Altered Sweating &lt;br /&gt;
Cold Hands and Feet &lt;br /&gt;
Tumor of Neural Crest Origin&lt;/p&gt;
&lt;p&gt;Abnormal Brain &lt;span class="caps"&gt;MRI&lt;/span&gt; Scans &lt;br /&gt;
Seizure &lt;br /&gt;
Enuresis &lt;br /&gt;
Hypotonia&lt;/p&gt;</general-symptoms>
    <general-test>&lt;p&gt;There are no tests for &lt;span class="caps"&gt;ROHHAD&lt;/span&gt; at this time.  Usually child exhibits multiple symptoms that may go undiagnosed until respiratory arrest occurs.&lt;/p&gt;</general-test>
    <general-treatment>&lt;p&gt;There are no treatments or cures for &lt;span class="caps"&gt;ROHHAD&lt;/span&gt;.&lt;/p&gt;</general-treatment>
    <id type="integer">1306</id>
    <name>Rapid-onset Obesity with Hypothalamic dysfunction, Hypoventilation and Autonomic Dysregulation</name>
    <participations-count type="integer">6</participations-count>
    <permalink>rapid-onset-obesity-with-hypothalamic-dysfunction--hypoventilation-and-autonomic-dysregulation</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal">30.0</prevalence-number>
    <prevalence-number-source-url>http://pediatrics.aappublications.org/cgi/content/full/120/1/e179</prevalence-number-source-url>
    <prevalence-type>Cases</prevalence-type>
    <prognosis></prognosis>
    <symptoms-count type="integer" nil="true"></symptoms-count>
    <synonym-tags>ROHHAD Syndrome</synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2009-05-05T02:39:12+00:00</updated-at>
  </community>
  <community>
    <causes></causes>
    <created-at type="datetime">2008-11-09T15:17:30+00:00</created-at>
    <description>&lt;p&gt;Raynaud&amp;#8217;s Disease is a disorder characterized by some areas of the body, including fingers, toes, the nose, and ears to feel numb and cool in response to cold temperatures or stress.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Raynaud&amp;#8217;s Disease is a disorder characterized by some areas of the body (fingers, toes, nose, ears, etc.) feeling numb and cool in response to cold temperatures or stress. This is caused by limited blood circulation to the affected areas due to the narrowing of arteries that supply blood to your skin.&lt;/p&gt;</disorder-description>
    <expert-id type="integer" nil="true"></expert-id>
    <general-symptoms></general-symptoms>
    <general-test></general-test>
    <general-treatment></general-treatment>
    <id type="integer">1244</id>
    <name>Raynaud's Disease</name>
    <participations-count type="integer">5</participations-count>
    <permalink>raynaud-s-disease</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal" nil="true"></prevalence-number>
    <prevalence-number-source-url></prevalence-number-source-url>
    <prevalence-type>Per 100,000 Population</prevalence-type>
    <prognosis></prognosis>
    <symptoms-count type="integer" nil="true"></symptoms-count>
    <synonym-tags>Raynaud Disease, Raynauds Disease </synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2009-08-07T03:44:53+00:00</updated-at>
  </community>
  <community>
    <causes></causes>
    <created-at type="datetime">2008-12-31T03:30:01+00:00</created-at>
    <description>&lt;p&gt;Reactive Arthritis is an autoimmune condition  due to an infection in another part of the body.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Reactive Arthritis is an autoimmune condition  due to an infection in another part of the body.&lt;/p&gt;</disorder-description>
    <expert-id type="integer" nil="true"></expert-id>
    <general-symptoms></general-symptoms>
    <general-test></general-test>
    <general-treatment></general-treatment>
    <id type="integer">1301</id>
    <name>Reactive Arthritis</name>
    <participations-count type="integer">2</participations-count>
    <permalink>reactive-arthritis</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal" nil="true"></prevalence-number>
    <prevalence-number-source-url></prevalence-number-source-url>
    <prevalence-type>Per 100,000 Population</prevalence-type>
    <prognosis></prognosis>
    <symptoms-count type="integer" nil="true"></symptoms-count>
    <synonym-tags>ReA</synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">1</topics-count>
    <updated-at type="datetime">2009-12-07T05:03:02+00:00</updated-at>
  </community>
  <community>
    <causes>&lt;p&gt;Pericarditis can be caused by a heart attack, bacterial, viral or fungal infections or a tumour or cancer spreading from nearby lungs or breasts.&lt;/p&gt;</causes>
    <created-at type="datetime">2008-07-04T05:45:27+00:00</created-at>
    <description>&lt;p&gt;Pericarditis is a condition caused by the inflammation of the lining surrounding the heart.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Pericarditis is a condition caused by the inflammation of the lining surrounding the heart.&lt;/p&gt;</disorder-description>
    <expert-id type="integer" nil="true"></expert-id>
    <general-symptoms>&lt;p&gt;There are a number of symptoms that effect patients with Recurrent Pericarditis.&lt;/p&gt;</general-symptoms>
    <general-test></general-test>
    <general-treatment></general-treatment>
    <id type="integer">1126</id>
    <name>Recurrent Pericarditis </name>
    <participations-count type="integer">1</participations-count>
    <permalink>recurrent-pericarditis</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal" nil="true"></prevalence-number>
    <prevalence-number-source-url></prevalence-number-source-url>
    <prevalence-type>Per 100,000 Population</prevalence-type>
    <prognosis></prognosis>
    <symptoms-count type="integer" nil="true"></symptoms-count>
    <synonym-tags>Recurring pericarditis, Accute pericarditis</synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">1</topics-count>
    <updated-at type="datetime">2008-07-15T13:15:29+00:00</updated-at>
  </community>
  <community>
    <causes></causes>
    <created-at type="datetime">2008-05-21T13:25:35+00:00</created-at>
    <description>&lt;p&gt;Refsum&amp;#8217;s Disease is a rare neurological disease resulting in the malformation of myelin sheaths around nerve cells.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Refsum&amp;#8217;s Disease is a rare neurological disease resulting in the malformation of myelin sheaths around nerve cells.&lt;/p&gt;</disorder-description>
    <expert-id type="integer" nil="true"></expert-id>
    <general-symptoms></general-symptoms>
    <general-test></general-test>
    <general-treatment></general-treatment>
    <id type="integer">1018</id>
    <name>Refsum's Disease</name>
    <participations-count type="integer">0</participations-count>
    <permalink>refsum-s-disease</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal">0.1</prevalence-number>
    <prevalence-number-source-url>http://www.orpha.net</prevalence-number-source-url>
    <prevalence-type>Per 100,000 Population</prevalence-type>
    <prognosis></prognosis>
    <symptoms-count type="integer" nil="true"></symptoms-count>
    <synonym-tags>Refsums Disease, Refsum Disease, Refsum-Thi&#233;baut disease, Refsum-Thi&#233;baut-Klenk-Kahlke disease, Heredopathia atactica polyneuritiformis</synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2009-07-20T20:12:34+00:00</updated-at>
  </community>
  <community>
    <causes></causes>
    <created-at type="datetime">2008-05-21T13:25:33+00:00</created-at>
    <description>&lt;p&gt;Relapsing polychondritis is a rare disorder characterized by the deterioration of the cartilage.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Relapsing polychondritis is a rare disorder characterized by the deterioration of the cartilage.&lt;/p&gt;</disorder-description>
    <expert-id type="integer" nil="true"></expert-id>
    <general-symptoms></general-symptoms>
    <general-test></general-test>
    <general-treatment></general-treatment>
    <id type="integer">755</id>
    <name>Relapsing Polychondritis</name>
    <participations-count type="integer">0</participations-count>
    <permalink>relapsing-polychondritis</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal">3.5</prevalence-number>
    <prevalence-number-source-url>http://www.orpha.net</prevalence-number-source-url>
    <prevalence-type>Per 100,000 Population</prevalence-type>
    <prognosis></prognosis>
    <symptoms-count type="integer" nil="true"></symptoms-count>
    <synonym-tags>chronic atrophic polychondritis, Meyenburg-Altherr-Uehlinger syndrome, von Meyenburg's disease, generalized chondromalacia, systemic chondromalacia</synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2009-06-12T18:11:31+00:00</updated-at>
  </community>
  <community>
    <causes nil="true"></causes>
    <created-at type="datetime">2008-05-21T13:25:32+00:00</created-at>
    <description nil="true"></description>
    <diagnosis nil="true"></diagnosis>
    <disorder-description nil="true"></disorder-description>
    <expert-id type="integer" nil="true"></expert-id>
    <general-symptoms nil="true"></general-symptoms>
    <general-test nil="true"></general-test>
    <general-treatment nil="true"></general-treatment>
    <id type="integer">556</id>
    <name>Renal adysplasia</name>
    <participations-count type="integer">0</participations-count>
    <permalink>renal-adysplasia</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal">26.0</prevalence-number>
    <prevalence-number-source-url>http://www.orpha.net</prevalence-number-source-url>
    <prevalence-type>Per 100,000 Population</prevalence-type>
    <prognosis nil="true"></prognosis>
    <symptoms-count type="integer" nil="true"></symptoms-count>
    <synonym-tags nil="true"></synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2008-05-21T13:25:32+00:00</updated-at>
  </community>
  <community>
    <causes></causes>
    <created-at type="datetime">2008-05-21T13:25:33+00:00</created-at>
    <description></description>
    <diagnosis></diagnosis>
    <disorder-description></disorder-description>
    <expert-id type="integer" nil="true"></expert-id>
    <general-symptoms></general-symptoms>
    <general-test></general-test>
    <general-treatment></general-treatment>
    <id type="integer">756</id>
    <name>Rendu-Osler-Weber Disease</name>
    <participations-count type="integer">0</participations-count>
    <permalink>rendu-osler-weber-disease</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal">3.5</prevalence-number>
    <prevalence-number-source-url>http://www.orpha.net</prevalence-number-source-url>
    <prevalence-type>Per 100,000 Population</prevalence-type>
    <prognosis></prognosis>
    <symptoms-count type="integer" nil="true"></symptoms-count>
    <synonym-tags>Rendu Osler Weber Disease, hereditary hemorrhagic telangiectasia, Osler's disease, Oslers disease</synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2009-08-07T03:47:41+00:00</updated-at>
  </community>
  <community>
    <causes></causes>
    <created-at type="datetime">2008-05-21T13:25:34+00:00</created-at>
    <description>&lt;p&gt;Restrictive Cardiomyopathy is a rare form of cardiomyopathy.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Restrictive Cardiomyopathy is a rare form of cardiomyopathy.&lt;/p&gt;</disorder-description>
    <expert-id type="integer" nil="true"></expert-id>
    <general-symptoms></general-symptoms>
    <general-test></general-test>
    <general-treatment></general-treatment>
    <id type="integer">791</id>
    <name>Restrictive Cardiomyopathy</name>
    <participations-count type="integer">3</participations-count>
    <permalink>restrictive-cardiomyopathy</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal">2.5</prevalence-number>
    <prevalence-number-source-url>http://www.orpha.net</prevalence-number-source-url>
    <prevalence-type>Per 100,000 Population</prevalence-type>
    <prognosis></prognosis>
    <symptoms-count type="integer" nil="true"></symptoms-count>
    <synonym-tags>RCM, Restrictive Cardiomyopathy, Idiopathic, Restrictive Cardiomyopathy, Familial, Idiopathic Restrictive Cardiomyopathy, Familial Restrictive Cardiomyopathy</synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2008-10-13T14:31:44+00:00</updated-at>
  </community>
  <community>
    <causes></causes>
    <created-at type="datetime">2008-05-21T13:25:32+00:00</created-at>
    <description></description>
    <diagnosis></diagnosis>
    <disorder-description></disorder-description>
    <expert-id type="integer" nil="true"></expert-id>
    <general-symptoms></general-symptoms>
    <general-test></general-test>
    <general-treatment></general-treatment>
    <id type="integer">552</id>
    <name>Retinitis Pigmentosa</name>
    <participations-count type="integer">3</participations-count>
    <permalink>retinitis-pigmentosa</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal">27.5</prevalence-number>
    <prevalence-number-source-url>http://www.orpha.net</prevalence-number-source-url>
    <prevalence-type>Per 100,000 Population</prevalence-type>
    <prognosis></prognosis>
    <symptoms-count type="integer" nil="true"></symptoms-count>
    <synonym-tags></synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2008-09-09T21:48:16+00:00</updated-at>
  </community>
  <community>
    <causes></causes>
    <created-at type="datetime">2008-05-21T13:25:33+00:00</created-at>
    <description>&lt;p&gt;Retinoblastoma is a rare form of cancer which develops in the cells of the retina.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Retinoblastoma is a rare form of cancer which develops in the cells of the retina.&lt;/p&gt;</disorder-description>
    <expert-id type="integer" nil="true"></expert-id>
    <general-symptoms></general-symptoms>
    <general-test></general-test>
    <general-treatment></general-treatment>
    <id type="integer">700</id>
    <name>Retinoblastoma</name>
    <participations-count type="integer">0</participations-count>
    <permalink>retinoblastoma</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal">5.4</prevalence-number>
    <prevalence-number-source-url>http://www.orpha.net</prevalence-number-source-url>
    <prevalence-type>Per 100,000 Population</prevalence-type>
    <prognosis></prognosis>
    <symptoms-count type="integer" nil="true"></symptoms-count>
    <synonym-tags>Rb</synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2009-08-05T02:51:47+00:00</updated-at>
  </community>
  <community>
    <causes></causes>
    <created-at type="datetime">2009-02-18T20:59:56+00:00</created-at>
    <description>&lt;p&gt;Retroperitoneal Fibrosis is an ideopathic auto-immune disorder that causes scar tissue to form in the the abdomen and wrap itself around the abdominal aorta. It can grow in thickness and length, and extend to vital organs, compromising their functions and causing pain.&lt;/p&gt;</description>
    <diagnosis></diagnosis>
    <disorder-description>&lt;p&gt;Retroperitoneal Fibrosis is an ideopathic auto-immune disorder that causes scar tissue to form in the the abdomen and wrap itself around the abdominal aorta. It can grow in thickness and length, and extend to vital organs, compromising their functions and causing pain.&lt;/p&gt;</disorder-description>
    <expert-id type="integer" nil="true"></expert-id>
    <general-symptoms></general-symptoms>
    <general-test></general-test>
    <general-treatment>&lt;p&gt;Prendisone is among the few drugs that have been shown to slow progression of the disease.&lt;/p&gt;</general-treatment>
    <id type="integer">1344</id>
    <name>Retroperitoneal Fibrosis</name>
    <participations-count type="integer">2</participations-count>
    <permalink>retroperitoneal-fibrosis</permalink>
    <posts-count type="integer">0</posts-count>
    <prevalence-number type="decimal" nil="true"></prevalence-number>
    <prevalence-number-source-url></prevalence-number-source-url>
    <prevalence-type>Per 100,000 Population</prevalence-type>
    <prognosis></prognosis>
    <symptoms-count type="integer" nil="true"></symptoms-count>
    <synonym-tags>Ormond's disease, Ormonds disease</synonym-tags>
    <synonyms-count type="integer">0</synonyms-count>
    <topics-count type="integer">0</topics-count>
    <updated-at type="datetime">2009-02-18T20:59:56+00:00</updated-at>
  </community>
</communities>
