3-methylglutaconic aciduria type 1

MONDO:0009610

3-methylglutaconic aciduria (3-MGA) type I is an inborn error of leucine metabolism with a variable clinical phenotype ranging from mildly delayed speech to psychomotor retardation, coma, failure to thrive, metabolic acidosis and dystonia.

Also known as: 3-methylglutaconic aciduria caused by mutation in AUH, 3-methylglutaconic aciduria caused by mutation in auh, 3-methylglutaconic aciduria type 1, 3-methylglutaconyl-CoA hydratase deficiency, 3MG-CoA hydratase deficiency, AUH 3-methylglutaconic aciduria, MGA1, auh 3-methylglutaconic aciduria

24 clinical trials for this condition and its sub-types.

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