3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome

Any 3-methylglutaconic aciduria in which the cause of the disease is a mutation in the SERAC1 gene.

Also known as: 3-methylglutaconic aciduria caused by mutation in SERAC1, 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome, 3-methylglutaconic aciduria with deafness-encephalopathy-Leigh-like syndrome, MEGDEL, MEGDEL syndrome, MGCA6, SERAC1 3-methylglutaconic aciduria, 3-MGCA type IV (formerly)

13 clinical trials for this condition and its sub-types, 0 tagged with 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome itself.