Fat transport deficiency explains rare childhood metabolic crises
Researchers studying a protein linked to a rare but severe disease have made a discovery that sheds light on how cells meet ...
Nature6y
The electron transport system (ETS) in the inner mitochondrial membrane.
the complex formed by acyl-CoA dehydrogenase, electron transfer flavoprotein (ETFP), and ETFP-ubiquinone oxidoreductase in yellow and orange; ubiquinone in green labeled with a Q; cytochrome c ...
Medical Dialogues6d
Medical Bulletin 04/ March/ 2025 - Video
Fat Transport Deficiency Unveiled as Key Factor in Rare Childhood Metabolic CrisesResearchers studying a protein linked to a ...
Medscape3d
Not So Rare: Errors of Metabolism During the Neonatal Period
CSPD, carbamyl phosphate synthetase deficiency; HHH, hyperornithinemia hyperammonemia homocitrullinuria syndrome; IVA, isovalemic acidemia; LCHADD, long chain 3-chydroxy-acyl-CoA dehydrogenase ...
Verywell Health on MSN1y
How Serious Is MCAD Deficiency?
Today, testing for MCAD deficiency is part of standard newborn screenings in the United States. When diagnosed promptly, MCAD ...