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<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/"><rdf:Description rdf:about="https://dirros.openscience.si/IzpisGradiva.php?id=24664"><dc:title>Sudden death of a four-day-old newborn due to mitochondrial trifunctional protein/long-chain 3-hydroxyacyl-coa dehydrogenase deficiencies and a systematic literature review of early deaths of neonates with fatty acid oxidation disorders</dc:title><dc:creator>Drole Torkar,	Ana	(Avtor)
	</dc:creator><dc:creator>Klinc,	Ana	(Avtor)
	</dc:creator><dc:creator>Remec,	Žiga Iztok	(Avtor)
	</dc:creator><dc:creator>Ranković,	Branislava	(Avtor)
	</dc:creator><dc:creator>Bartolj,	Klara	(Avtor)
	</dc:creator><dc:creator>Bertok,	Sara	(Avtor)
	</dc:creator><dc:creator>Colja,	Sara	(Avtor)
	</dc:creator><dc:creator>Čuk,	Vanja	(Avtor)
	</dc:creator><dc:creator>Debeljak,	Maruša	(Avtor)
	</dc:creator><dc:creator>Kozjek,	Eva	(Avtor)
	</dc:creator><dc:creator>Repič-Lampret,	Barbka	(Avtor)
	</dc:creator><dc:creator>Mlinarič,	Matej	(Avtor)
	</dc:creator><dc:creator>Mohar Hajnšek,	Tinka	(Avtor)
	</dc:creator><dc:creator>Perko,	Daša	(Avtor)
	</dc:creator><dc:creator>Štajer,	Katarina	(Avtor)
	</dc:creator><dc:creator>Tesovnik,	Tine	(Avtor)
	</dc:creator><dc:creator>Trampuž,	Domen	(Avtor)
	</dc:creator><dc:creator>Ulaga,	Blanka	(Avtor)
	</dc:creator><dc:creator>Kovač,	Jernej	(Avtor)
	</dc:creator><dc:creator>Battelino,	Tadej	(Avtor)
	</dc:creator><dc:creator>Žerjav-Tanšek,	Mojca	(Avtor)
	</dc:creator><dc:creator>Grošelj,	Urh	(Avtor)
	</dc:creator><dc:subject>FAOD</dc:subject><dc:subject>LCHAD deficiency</dc:subject><dc:subject>LCHADD</dc:subject><dc:subject>MTP deficiency</dc:subject><dc:subject>MTPD</dc:subject><dc:subject>NBS</dc:subject><dc:subject>fatty acid oxidation disorder</dc:subject><dc:subject>newborn</dc:subject><dc:subject>newborn screening</dc:subject><dc:subject>sudden infant death</dc:subject><dc:description>Mitochondrial trifunctional protein (MTP) and long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiencies have been a part of the Slovenian newborn screening (NBS) program since 2018. We describe a case of early lethal presentation of MTPD/LCHADD in a term newborn. The girl was born after an uneventful pregnancy and delivery, and she was discharged home at the age of 3 days, appearing well. At the age of 4 days, she was found without signs of life. Resuscitation was not successful. The NBS test performed using tandem mass spectrometry (MS/MS) showed a positive screen for MTPD/LCHADD. Genetic analysis performed on a dried blood spot (DBS) sample identified two heterozygous variants in the HADHA gene: a nucleotide duplication introducing a premature termination codon (p.Arg205Ter) and a nucleotide substitution (p.Glu510Gln). Post-mortem studies showed massive macro-vesicular fat accumulation in the liver and, to a smaller extent, in the heart, consistent with MTPD/LCHADD. A neonatal acute cardiac presentation resulting in demise was suspected. We conducted a systematic literature review of early neonatal deaths within 14 days postpartum attributed to confirmed fatty acid oxidation disorders (FAODs), which are estimated to account for 5% of sudden infant deaths. We discuss the pitfalls of the NBS for MTPD/LCHADD.</dc:description><dc:date>2025</dc:date><dc:date>2025-12-11 08:46:01</dc:date><dc:type>Neznano</dc:type><dc:identifier>24664</dc:identifier><dc:language>sl</dc:language></rdf:Description></rdf:RDF>
