Congenital amino acid metabolism disorders are one of three rare congenital metabolic disorders in newborns. There is no cure for the disease, treatment methods only aim to limit the signs of the disease.

If congenital urea metabolism disorder is not detected early and treated promptly, it can lead to serious complications, even death. Currently, there is no radical cure for the disease, the main treatment methods include: Reducing the concentration of nitrogen in the blood serum, reducing the consumption of foods containing nitrogen in the diet, etc.