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.

Connect. Empower. Inspire.