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		<title>Genes Behind a Rare Heart-Filling Disorder Point Toward Personalized Care</title>
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		<pubDate>Tue, 27 Oct 2026 00:08:43 +0000</pubDate>
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		<category><![CDATA[cardiac amyloidosis]]></category>
		<category><![CDATA[dilated cardiomyopathy]]></category>
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		<category><![CDATA[hypertrophic cardiomyopathy]]></category>
		<category><![CDATA[LAMP2]]></category>
		<category><![CDATA[MYBPC3]]></category>
		<category><![CDATA[restrictive cardiomyopathy]]></category>
		<category><![CDATA[TTR]]></category>
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					<description><![CDATA[Whole-exome sequencing of 568 cardiomyopathy patients found pathogenic variants in nearly three-quarters of those with restrictive filling physiology, with MYBPC3, TTR, and LAMP2 emerging as key genes.]]></description>
		
		
		
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		<title>Rare LAMP2 Variants Behind Severe Heart Disease in Two Young Women Misdiagnosed as Amyloidosis</title>
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		<pubDate>Tue, 27 Oct 2026 00:01:10 +0000</pubDate>
				<category><![CDATA[Health]]></category>
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		<category><![CDATA[cardiac amyloidosis]]></category>
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		<category><![CDATA[case report]]></category>
		<category><![CDATA[Danon disease]]></category>
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		<category><![CDATA[Genetic Testing]]></category>
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					<description><![CDATA[A case report describes two Chinese women with severe Danon disease initially suspected of cardiac amyloidosis, diagnosed through biopsy and two rare LAMP2 variants.]]></description>
		
		
		
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