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									<identifier>oai:www.peertechzpublications.org:10.17352/2455-2283.000057</identifier>
									<datestamp>2018-11-06</datestamp>
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									<oai_dc:dc xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:mml="http://www.w3.org/1998/Math/MathML" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
										<dc:title>
										Primary Intestinal Lymphangiectasia diagnosed by Single-Balloon Enteroscopy
										</dc:title><dc:creator>C Romero Mascarell</dc:creator><dc:creator> IK Araujo</dc:creator><dc:creator> I Ordás</dc:creator><dc:creator> H Briceno</dc:creator><dc:creator> D Monfort</dc:creator><dc:creator> C Rodriguez-de Miguel</dc:creator><dc:creator> A Ginés</dc:creator><dc:creator> G Fernández-Esparrach</dc:creator><dc:creator> M Cuatrecasas</dc:creator><dc:creator> J Llach</dc:creator><dc:creator/><dc:creator>B González Suárez</dc:creator><dc:description>&lt;p&gt;Primary intestinal lymphangiectasia (PIL) is a rare protein losing gastroenteropathy that usually affects children and teenagers. There are only a few cases described in the literature. The diagnosis is confirmed by the presence of intestinal lymphangiectasia based on endoscopic findings and histology.&lt;/p&gt;&lt;p&gt;We present a case of PIL diagnosed in a teenager patient, by Small Bowel Capsule Endoscopy (SBCE) and Single Balloon Enteroscopy (SBE).&lt;/p&gt;</dc:description>
										<dc:publisher>Archives of Clinical Gastroenterology - Peertechz Publications</dc:publisher>
										<dc:date>2018-11-06</dc:date>
										<dc:type>Case Report</dc:type>
										<dc:identifier>https://doi.org/10.17352/2455-2283.000057</dc:identifier>
										<dc:language>en</dc:language>
										<dc:rights>Copyright © C Romero Mascarell et al.</dc:rights>
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