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	<title>neonatal hypophosphatasia &#8211; BIOENGINEER.ORG</title>
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		<title>Neonatal Hypophosphatasia: Unraveling a Rare Genetic Disorder</title>
		<link>https://bioengineer.org/neonatal-hypophosphatasia-unraveling-a-rare-genetic-disorder/</link>
		
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		<pubDate>Thu, 23 Oct 2025 14:35:25 +0000</pubDate>
				<category><![CDATA[Health]]></category>
		<category><![CDATA[ALPL gene mutations]]></category>
		<category><![CDATA[early diagnosis]]></category>
		<category><![CDATA[neonatal hypophosphatasia]]></category>
		<category><![CDATA[rare genetic disorders]]></category>
		<category><![CDATA[skeletal abnormalities]]></category>
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					<description><![CDATA[In a striking revelation in pediatric medicine, a recent case report has highlighted neonatal hypophosphatasia, an exceptionally rare genetic disorder that poses significant challenges for early diagnosis and management. The findings from Vohra, Chohan, and Mirza illuminate the intricate complexities of this condition, showcasing the necessity for heightened clinical awareness and prompt interventions. Their study, [&#8230;]]]></description>
		
		
		
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