<?xml version="1.0" encoding="UTF-8"?><rss xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:content="http://purl.org/rss/1.0/modules/content/" xmlns:atom="http://www.w3.org/2005/Atom" version="2.0"><channel><title><![CDATA[RSS Feed]]></title><description><![CDATA[RSS Feed]]></description><link>http://direct.ecency.com</link><image><url>http://direct.ecency.com/logo512.png</url><title>RSS Feed</title><link>http://direct.ecency.com</link></image><generator>RSS for Node</generator><lastBuildDate>Tue, 21 Apr 2026 18:40:23 GMT</lastBuildDate><atom:link href="http://direct.ecency.com/created/1p36/rss.xml" rel="self" type="application/rss+xml"/><item><title><![CDATA[1p36 deletion syndrome]]></title><description><![CDATA[1p36 deletion syndrome (also known as monosomy 1p36) is a congenital genetic disorder characterized by moderate to severe intellectual disability, delayed growth, hypotonia, seizures, limited speech ability,]]></description><link>http://direct.ecency.com/1p36/@karthikmbbs2/1p36-deletion-syndrome-55c30c94f8b6e</link><guid isPermaLink="true">http://direct.ecency.com/1p36/@karthikmbbs2/1p36-deletion-syndrome-55c30c94f8b6e</guid><category><![CDATA[1p36]]></category><dc:creator><![CDATA[karthikmbbs2]]></dc:creator><pubDate>Sun, 06 May 2018 07:15:36 GMT</pubDate><enclosure url="https://images.ecency.com/p/o1AJ9qDyyJNSpZWhUgGYc3MngFqoAN28U6BHQTxhn7MHcBs8A?format=match&amp;mode=fit" length="0" type="false"/></item></channel></rss>