3 Methylglutaconic Aciduria Type IV
Type of disease: Rare conditions
3-methylglutaconic aciduria (3-MGA) Type IV is an inherited condition present in individuals with increased 3-MGA acid excretion that do not fall under the other three categories of 3-MGA. Type IV usually presents itself during infancy through seizures, decreased muscle tone, developmental delay, retardation, and severe failure to grow. There is no known treatment for this condition.