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<oembed><version>1.0</version><provider_name>Institut de Myologie</provider_name><provider_url>https://www.institut-myologie.org/en/</provider_url><author_name>Anne Berthomier</author_name><author_url>https://www.institut-myologie.org/en/author/aberthomier/</author_url><title>Expanding the myopathological spectrum of calpainopathies - Institut de Myologie</title><type>rich</type><width>600</width><height>338</height><html>&lt;blockquote class="wp-embedded-content" data-secret="IKP3eb7ivJ"&gt;&lt;a href="https://www.institut-myologie.org/en/2017/07/16/expanding-myopathological-spectrum-calpainopathies/"&gt;Expanding the myopathological spectrum of calpainopathies&lt;/a&gt;&lt;/blockquote&gt;&lt;iframe sandbox="allow-scripts" security="restricted" src="https://www.institut-myologie.org/en/2017/07/16/expanding-myopathological-spectrum-calpainopathies/embed/#?secret=IKP3eb7ivJ" width="600" height="338" title="&#x201C;Expanding the myopathological spectrum of calpainopathies&#x201D; &#x2014; Institut de Myologie" data-secret="IKP3eb7ivJ" 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>Mutations in calpain-3 cause limb girdle muscular dystrophy 2A. Biopsy pathology is typically dystrophic, sometimes characteriSed by frequent lobulated fibres. More recently calpain mutations have been shown in association with eosinophilic myositis, suggesting that calpain mutations may render muscle susceptible to inflammatory change. This article presents the case of a 33-year old female with mild &hellip; [Read more]</description></oembed>
