| Literature DB >> 26409463 |
Clément Pontoizeau1,2, Florence Habarou3,4,5, Anaïs Brassier3, Alice Veauville-Merllié6, Coraline Grisel3, Jean-Baptiste Arnoux3, Christine Vianey-Saban6, Robert Barouki3,4,5, Bernadette Chadefaux-Vekemans3,4,5, Cécile Acquaviva6, Pascale de Lonlay3, Chris Ottolenghi3,4,5.
Abstract
Classical neonatal-onset glutaric aciduria type 2 (MAD deficiency) is a severe disorder of mitochondrial fatty acid oxidation associated with poor survival. Secondary dysfunction of acyl-CoA dehydrogenases may result from deficiency for riboflavin transporters, leading to severe disorders that, nevertheless, are treatable by riboflavin supplementation. In the last 10 years, we identified nine newborns with biochemical features consistent with MAD deficiency, only four of whom survived past the neonatal period. A likely iatrogenic cause of riboflavin deficiency was found in two premature newborns having parenteral nutrition, one of whom recovered upon multivitamin supplementation, whereas the other died before diagnosis. Four other patients had demonstrated mutations involving ETF or ETF-DH flavoproteins, whereas the remaining three patients presumably had secondary deficiencies of unknown mechanism. Interestingly, six newborns among the seven tested for plasma amino acids had pronounced hyperprolinemia. In one case, because the initial diagnostic workup did not include organic acids and acylcarnitine profiling, clinical presentation and hyperprolinemia suggested the diagnosis. Analysis of our full cohort of >50,000 samples from >30,000 patients suggests that the proline/alanine ratio may be a good marker of MAD deficiency and could contribute to a more effective management of the treatable forms.Entities:
Year: 2015 PMID: 26409463 PMCID: PMC4864717 DOI: 10.1007/8904_2015_481
Source DB: PubMed Journal: JIMD Rep ISSN: 2192-8304