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<title>OWL: OCOSH Classification/Joint Diseases/Arthrogryposis</title>
<link>http://www.orthopaedicweblinks.com</link>
<description>Arthrogryposis</description>
<language>en-us</language>
<lastBuildDate>Sun Jan 13 2008 17:14:53 GMT</lastBuildDate>
<copyright>Copyright 2005 OWL Inc.</copyright>
<managingEditor>orthopaedicweblinks@gmail.com (Christian Veillette)</managingEditor>
<webMaster>orthopaedicweblinks@gmail.com (OWL Inc.)</webMaster>
<item>
<title>Arthrogryposis Multiplex Congenita</title>
<link>http://www.orthopaedicweblinks.com/Detailed/218.html</link>
<description>Web site of a support group for this joint condition </description>
<pubDate>2002-01-11 17:14:53 GMT</pubDate>
<guid isPermaLink="false">http://www.orthopaedicweblinks.com/cgi-bin/owl/jump.cgi?ID=218</guid>
<author>Melissa Schmidt</author>
</item><item>
<title>Wheeless Arthrogryposis Multiplex Congenita Amyoplasia</title>
<link>http://www.orthopaedicweblinks.com/Detailed/10542.html</link>
<description>musculoskeletal dz is characterized by congenital immobility of multiple joints.
&lt;br&gt;    - there may be as many as 10 to 20 specific arthrogrypotic disorders, all with similar joint manifestations;
&lt;br&gt;    - believed to be caused by oligohydrmnios &amp; conditions limiting fetal movement;
&lt;br&gt;    - joint develops in arthrogryposis multiplex congenita, but periarticular soft tissue structures
 become fibrotic, leading to development of an incomplete fibrous ankylosis;
</description>
<pubDate>2006-12-11 17:14:53 GMT</pubDate>
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<author>Wheeless</author>
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