Very long-chain acyl-CoA dehydrogenase deficiency revisited: a retrospective genotype–phenotype analysis in a Saudi tertiary center

IntroductionIn this retrospective study, we analyzed clinical, biochemical, and genetic data and examined correlations between prevalent variants and outcomes of very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency.MethodsPatients with VLCAD deficiency confirmed through molecular genetic testin...

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Bibliografiset tiedot

Päätekijät:	Suzan Suliman Alhumaidi, Fahad Abdulrahman Algaeed, Meshari Fayez Aladhadh, Sara Abdulrahman Alkaff
Aineistotyyppi:	Artigo
Kieli:	Inglês
Julkaistu:	Frontiers Media S.A. 2025-05-01
Sarja:	Frontiers in Genetics
Aiheet:	clinical characteristics clinical molecular Saudi Arabia VLCAD deficiency genotype-phenotype correlation
Linkit:	https://www.frontiersin.org/articles/10.3389/fgene.2025.1584817/full
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