transient neonatal multiple acyl-CoA dehydrogenase deficiency
Findings
No curated finding names transient neonatal multiple acyl-CoA dehydrogenase deficiency yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
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.
Definition from the Mondo Disease Ontology (MONDO:0018014), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
Other names
4 names
Resolves to: transient neonatal multiple acyl-CoA dehydrogenase deficiency
- Also called
- transient neonatal glutaric acidemia type 2transient neonatal glutaric aciduria type 2transient neonatal MAD deficiencytransient neonatal MADD