/3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome
Rare Disease
MONDO:0013875
Also Known As
3-methylglutaconic aciduria caused by mutation in SERAC13-methylglutaconic aciduria type 63-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome3-methylglutaconic aciduria with deafness-encephalopathy-Leigh-like syndromeMEGDELMEGDEL syndromeMGCA6SERAC1 3-methylglutaconic aciduria3-MGCA type IV (formerly)3-MGCA-4 (formerly)3-Methylglutaconic aciduria with dystonia-deafness, hepatopathy, encephalopathy, and Leigh-like syndrome3-Methylglutaconic aciduria, type 63-methylglutaconic aciduria type VISERAC1 defect
Definition
Any 3-methylglutaconic aciduria in which the cause of the disease is a mutation in the SERAC1 gene.
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