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<oembed><version>1.0</version><provider_name>Revista Brasileira de Oftalmologia</provider_name><provider_url>https://www.rbojournal.org/en/</provider_url><title>Electrophysiolocal findings in Mohr-Tranebj&#xE6;rg syndrome - Revista Brasileira de Oftalmologia</title><type>rich</type><width>600</width><height>338</height><html>&lt;blockquote class="wp-embedded-content" data-secret="QcWHTJzTZc"&gt;&lt;a href="https://www.rbojournal.org/en/article/electrophysiolocal-findings-in-mohr-tranebjaerg-syndrome/"&gt;Electrophysiolocal findings in Mohr-Tranebj&#xE6;rg syndrome&lt;/a&gt;&lt;/blockquote&gt;&lt;iframe sandbox="allow-scripts" security="restricted" src="https://www.rbojournal.org/en/article/electrophysiolocal-findings-in-mohr-tranebjaerg-syndrome/embed/#?secret=QcWHTJzTZc" width="600" height="338" title="&#x201C;Electrophysiolocal findings in Mohr-Tranebj&#xE6;rg syndrome&#x201D; &#x2014; Revista Brasileira de Oftalmologia" data-secret="QcWHTJzTZc" frameborder="0" marginwidth="0" marginheight="0" scrolling="no" class="wp-embedded-content"&gt;&lt;/iframe&gt;&lt;script type="text/javascript"&gt;
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</html><description>Mohr-Tranebj&#xE6;rg syndrome (MTS) is an X-liked recessive rare syndrome also known as deafness-dystonia syndrome. The severity of the symptoms may vary, but they progress usually to severe deafness and dystonia and sometimes they are accompanied by cortical deterioration of vision and mental deterioration. The purpose of this paper is to illustrate a very interesting case of Mohr-Tranebj&#xE6;rg syndrome. A 24-year-old italian man with Mohr-Tranebj&#xE6;rg syndrome underwent full field electroretinography (ERG) and visual evoked potentials (VEPs). Fundus examination showed apparently normal [...]</description></oembed>

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