<?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>https://alpha.ecency.com</link><image><url>https://alpha.ecency.com/logo512.png</url><title>RSS Feed</title><link>https://alpha.ecency.com</link></image><generator>RSS for Node</generator><lastBuildDate>Tue, 26 May 2026 15:54:58 GMT</lastBuildDate><atom:link href="https://alpha.ecency.com/@rasavel2/rss" rel="self" type="application/rss+xml"/><item><title><![CDATA[Aromatase excess syndrome]]></title><description><![CDATA[Aromatase excess syndrome (AES or AEXS), also sometimes referred to as familial hyperestrogenism or familial gynecomastia, is a rare genetic and endocrine syndrome which is characterized by an overexpression]]></description><link>https://alpha.ecency.com/aromatase/@rasavel2/aromatase-excess-syndrome-c913b70a42cb8</link><guid isPermaLink="true">https://alpha.ecency.com/aromatase/@rasavel2/aromatase-excess-syndrome-c913b70a42cb8</guid><category><![CDATA[aromatase]]></category><dc:creator><![CDATA[rasavel2]]></dc:creator><pubDate>Mon, 04 Jun 2018 17:54:51 GMT</pubDate></item><item><title><![CDATA[Antiphospholipid syndrome]]></title><description><![CDATA[Antiphospholipid syndrome or antiphospholipid antibody syndrome (APS or APLS), is an autoimmune, hypercoagulable state caused by antiphospholipid antibodies. APS provokes blood clots (thrombosis) in both]]></description><link>https://alpha.ecency.com/antiphospholipid/@rasavel2/antiphospholipid-syndrome-2cbb3d001af8b</link><guid isPermaLink="true">https://alpha.ecency.com/antiphospholipid/@rasavel2/antiphospholipid-syndrome-2cbb3d001af8b</guid><category><![CDATA[antiphospholipid]]></category><dc:creator><![CDATA[rasavel2]]></dc:creator><pubDate>Fri, 01 Jun 2018 15:46:21 GMT</pubDate></item><item><title><![CDATA[Andersen–Tawil syndrome]]></title><description><![CDATA[Andersen–Tawil syndrome, also called Andersen syndrome and Long QT syndrome 7, is a form of long QT syndrome.[1] It is a rare genetic disorder, and is inherited in an autosomal dominant pattern and predisposes]]></description><link>https://alpha.ecency.com/vincentb/@rasavel2/andersen-tawil-syndrome-d557a380afd7a</link><guid isPermaLink="true">https://alpha.ecency.com/vincentb/@rasavel2/andersen-tawil-syndrome-d557a380afd7a</guid><category><![CDATA[vincentb]]></category><dc:creator><![CDATA[rasavel2]]></dc:creator><pubDate>Wed, 30 May 2018 15:46:39 GMT</pubDate></item><item><title><![CDATA[Alopecia contractures dwarfism mental retardation syndrome]]></title><description><![CDATA[Alopecia contractures dwarfism mental retardation syndrome or (ACD mental retardation syndrome) is a developmental disorder which causes mainly baldness and dwarfism in combination with intellectual]]></description><link>https://alpha.ecency.com/syndrome/@rasavel2/alopecia-contractures-dwarfism-mental-retardation-syndrome-3594eaf71bd04</link><guid isPermaLink="true">https://alpha.ecency.com/syndrome/@rasavel2/alopecia-contractures-dwarfism-mental-retardation-syndrome-3594eaf71bd04</guid><category><![CDATA[syndrome]]></category><dc:creator><![CDATA[rasavel2]]></dc:creator><pubDate>Mon, 28 May 2018 16:59:12 GMT</pubDate></item><item><title><![CDATA[Albinism–deafness syndrome]]></title><description><![CDATA[Albinism–deafness syndrome (also known as "Woolf syndrome" and "Ziprkowski–Margolis syndrome") is a condition characterized by congenital neural deafness and a severe or extreme]]></description><link>https://alpha.ecency.com/albinismdeafness/@rasavel2/albinism-deafness-syndrome-73f67d8f704d8</link><guid isPermaLink="true">https://alpha.ecency.com/albinismdeafness/@rasavel2/albinism-deafness-syndrome-73f67d8f704d8</guid><category><![CDATA[albinismdeafness]]></category><dc:creator><![CDATA[rasavel2]]></dc:creator><pubDate>Fri, 25 May 2018 16:21:30 GMT</pubDate></item><item><title><![CDATA[Adult-onset immunodeficiency syndrome]]></title><description><![CDATA[Adult-onset immunodeficiency syndrome is a provisional name for a newly diagnosed immunodeficiency illness. The name is proposed in the first public study to identify the syndrome.[1] It appears to be]]></description><link>https://alpha.ecency.com/adult-onset/@rasavel2/adult-onset-immunodeficiency-syndrome-68f24ea69a012</link><guid isPermaLink="true">https://alpha.ecency.com/adult-onset/@rasavel2/adult-onset-immunodeficiency-syndrome-68f24ea69a012</guid><category><![CDATA[adult-onset]]></category><dc:creator><![CDATA[rasavel2]]></dc:creator><pubDate>Tue, 22 May 2018 15:34:06 GMT</pubDate></item><item><title><![CDATA[Stokes–Adams syndrome]]></title><description><![CDATA[Stokes–Adams syndrome (alternative eponyms include Adams–Stokes syndrome, Gerbezius–Morgagni–Adams–Stokes syndrome and Gerbec–Morgagni–Adams–Stokes syndrome)[1] is a periodic fainting spell in which there]]></description><link>https://alpha.ecency.com/stokesadams/@rasavel2/stokes-adams-syndrome-07a2eaa16f401</link><guid 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