has characteristic has characteristic Transient acyl-CoA dehydrogenase deficiency transient neonatal multiple acyl-CoA dehydrogenase deficiency https://www.malacards.org/card/transient_neonatal_multiple_acyl_coa_dehydrogenase_deficiency transient neonatal glutaric acidemia type 2 UMLS:C4509950 Orphanet:329942 Transient neonatal multiple acyl-CoA dehydrogenase deficiency describes a very rare condition where a maternal riboflavin deficiency causes an infant to present with manifestations similar to those seen in multiple acyl-CoA dehydrogenase (MAD) deficiency such as poor suck, metabolic acidosis and hypoglycemia, but that resolves completely with oral riboflavin. In the one patient described haploinsufficiency of the human riboflavin transporter (hRFT1) was described in the mother. GARD:0021498 MEDGEN:1373921 SCTID:723552005 transient neonatal glutaric aciduria type 2 transient neonatal MADD MONDO:0018014 transient neonatal MAD deficiency