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<oembed><version>1.0</version><provider_name>ERN ITHACA</provider_name><provider_url>https://ern-ithaca.eu/it</provider_url><author_name>ERN ITHACA</author_name><author_url>https://ern-ithaca.eu/it</author_url><title>Beckwith&#x2013;Wiedemann Guideline - ERN ITHACA</title><type>rich</type><width>600</width><height>338</height><html>&lt;blockquote class="wp-embedded-content" data-secret="TkfBPkz33r"&gt;&lt;a href="https://ern-ithaca.eu/it/guidelines/ern-ithaca-guidelines/beckwith-wiedemann-guideline/"&gt;Beckwith&#x2013;Wiedemann Guideline&lt;/a&gt;&lt;/blockquote&gt;&lt;iframe sandbox="allow-scripts" security="restricted" src="https://ern-ithaca.eu/it/guidelines/ern-ithaca-guidelines/beckwith-wiedemann-guideline/embed/#?secret=TkfBPkz33r" width="600" height="338" title="&#x201C;Beckwith&#x2013;Wiedemann Guideline&#x201D; &#x2014; ERN ITHACA" data-secret="TkfBPkz33r" frameborder="0" marginwidth="0" marginheight="0" scrolling="no" class="wp-embedded-content"&gt;&lt;/iframe&gt;&lt;script&gt;
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&lt;/script&gt;</html><description>This recommendation is aligned with the latest research findings available as of April 2018. Background Beckwith&#x2013;Wiedemann syndrome (BWS), a human genomic imprinting disorder, is characterized by phenotypic variability that might include overgrowth, macroglossia, abdominal wall defects, neonatal hypoglycaemia, lateralized overgrowth and predisposition to embryonal tumours. Delineation of the molecular defects within the imprinted 11p15.5 region [&hellip;]</description></oembed>
