Transient multiple acyl-CoA dehydrogenation deficiency in a newborn female caused by maternal riboflavin deficiency.

@article{Chiong2007TransientMA,
  title={Transient multiple acyl-CoA dehydrogenation deficiency in a newborn female caused by maternal riboflavin deficiency.},
  author={Mary Anne Chiong and Keow Giak Sim and Kevin T. Carpenter and William J. Rhead and Gloria Y. F. Ho and Rikke Katrine Jentoft Olsen and John Christodoulou},
  journal={Molecular genetics and metabolism},
  year={2007},
  volume={92 1-2},
  pages={
          109-14
        }
}
A newborn female presented on the first day of life with clinical and biochemical findings consistent with multiple acyl-CoA dehydrogenase deficiency (MADD). Riboflavin supplementation corrected the biochemical abnormalities 24 h after commencing the vitamin. In vitro acylcarnitine profiling in intact fibroblasts both in normal and riboflavin depleted media showed normal oxidation of fatty acids excluding defects in electron transfer flavoprotein (ETF), or ETF ubiquinone oxidoreductase (ETF:QO… CONTINUE READING

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