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	<title>NEXMIF / XLID-98 &#8211; Bergamo e Sport</title>
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		<title>&#8220;Un aiuto per i gemellini Liam e Theo, cure in USA&#8221;: l&#8217;appello condiviso da De Roon</title>
		<link>https://www.bergamoesport.it/un-aiuto-per-i-gemellini-liam-e-theo-cure-in-usa-lappello-condiviso-da-de-roon/?utm_source=rss&#038;utm_medium=rss&#038;utm_campaign=un-aiuto-per-i-gemellini-liam-e-theo-cure-in-usa-lappello-condiviso-da-de-roon</link>
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		<dc:creator><![CDATA[bergamoesport]]></dc:creator>
		<pubDate>Tue, 28 Oct 2025 11:40:23 +0000</pubDate>
				<category><![CDATA[Atalanta]]></category>
		<category><![CDATA[Calcio]]></category>
		<category><![CDATA[Highlight]]></category>
		<category><![CDATA[Sport vari]]></category>
		<category><![CDATA[cure]]></category>
		<category><![CDATA[donazioni]]></category>
		<category><![CDATA[Erica Tironi]]></category>
		<category><![CDATA[gemellini]]></category>
		<category><![CDATA[gene]]></category>
		<category><![CDATA[Gofoundme]]></category>
		<category><![CDATA[Heng-Ye Man]]></category>
		<category><![CDATA[Liam e Theo]]></category>
		<category><![CDATA[Marten de Roon]]></category>
		<category><![CDATA[mutazione genetica]]></category>
		<category><![CDATA[NEXMIF / XLID-98]]></category>
		<category><![CDATA[sottoscrizione]]></category>
		<category><![CDATA[USA]]></category>
		<guid isPermaLink="false">https://www.bergamoesport.it/?p=171956</guid>

					<description><![CDATA[Un appello social condiviso nelle stories e oltre da un bergamasco non di sangue ma di spirito come Marten de [&#8230;]]]></description>
										<content:encoded><![CDATA[<img style="margin-bottom:15px;width:100%;display:block;" src="https://bergamoesport.b-cdn.net/wp-content/uploads/2025/10/bambini-raro-morbo.jpeg"><p>Un <strong>appello social</strong> condiviso nelle stories e oltre da un bergamasco non di sangue ma di spirito come <strong>Marten de Roon</strong>, capitano e leader in campo dell&#8217;Atalanta, non ha più modo di passare inosservato. I <strong>gemellini</strong> bergamaschi <strong>Liam e Theo</strong>, che lottano &#8220;per camminare e per vivere&#8221; come recita il profilo Instagram loro dedicato, necessitano di cure costosissime negli Stati Uniti d&#8217;America, perché qui da noi non esistono strutture adeguatamente attrezzate.</p>
<p>La famiglia, con l&#8217;aiuto di amici come <strong>Beppe Motta</strong> di Elite Events, ha aperto una raccolta fondi sulla piattaforma Gofoundme cliccando <a href="https://www.gofundme.com/f/Theoelism?attribution_id=sl:de530721-537c-4c63-9bae-f74a7c42fb0e&amp;utm_campaign=natman_sharesheet_dash&amp;utm_medium=customer&amp;utm_source=copy_link">QUI</a>. I gemellini di <strong>Mapello</strong>, come scrive mamma <strong>Erica Tironi</strong> sulla piattaforma, sono affetti da una&nbsp;mutazione genetica rarissima: NEXMIF / XLID-98. &#8220;Un piccolo errore nel DNA con effetti molto grandi, che spegne&nbsp;piano piano le connessioni del cervello&#8221;.</p>
<div>Liam e Theo potrebbero non parlare, non camminare e non comprendere mai ciò che li circonda rischiando di&nbsp;sviluppare epilessia, autismo e una&nbsp;<strong>disabilità intellettiva profonda</strong>. A Bergamo, solo la diagnosi, perché non c&#8217;è cura. Negli Stati Uniti, invece, il dottor Heng-Ye Man e il suo team di ricercatori hanno dimostrato che la reintroduzione del gene NEXMIF può ripristinare le connessioni cerebrali nei modelli animali (studio pubblicato su Translational Psychiatry, 2025).</div>
<div>&nbsp;</div>
<div>È la prima prova concreta che una terapia genica per NEXMIF può funzionare. Ora serve trasformare quella scoperta in una cura reale per i bambini. Quando una malattia è rara, però,&nbsp;le aziende farmaceutiche non investono,&nbsp;i fondi pubblici non arrivano e&nbsp;<strong>le famiglie devono finanziare da sole la ricerca. Ogni donazione privata è vitale.</strong></div>
<div>&nbsp;</div>
<div>Le donazioni andranno:&nbsp;</div>
<ul>
<li>a<strong>&nbsp;finanziare la ricerca genetica del Dr. Man</strong> e il programma di sviluppo della terapia genica NEXMIF;</li>
<li>a sostenere lo studio sul&nbsp;<strong>riposizionamento di farmaci già esistenti;</strong></li>
<li>a garantire ai gemelli&nbsp;<strong>terapie fisioterapiche e neurologiche intensive,</strong> tutte a pagamento.&nbsp;</li>
</ul>
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<div style="color: #3897f0; font-family: Arial,sans-serif; font-size: 14px; font-style: normal; font-weight: 550; line-height: 18px;">Visualizza questo post su Instagram</div>
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<p style="color: #c9c8cd; font-family: Arial,sans-serif; font-size: 14px; line-height: 17px; margin-bottom: 0; margin-top: 8px; overflow: hidden; padding: 8px 0 7px; text-align: center; text-overflow: ellipsis; white-space: nowrap;"><a style="color: #c9c8cd; font-family: Arial,sans-serif; font-size: 14px; font-style: normal; font-weight: normal; line-height: 17px; text-decoration: none;" href="https://www.instagram.com/reel/DQR9rnwjCDN/?utm_source=ig_embed&amp;utm_campaign=loading" target="_blank" rel="noopener">Un post condiviso da Motta Giuseppe (@beppe.motta)</a></p>
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<em><strong>Esseffe</strong></em></p>
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