Phenylketonuria Treatment; Helps Terminate the Symptoms of PKU and Avoid Brain Damage
Phenylketonuria Treatment Phenylketonuria treatment includes a strict diet with limited protein. Phenylketonuria (PKU) is a rare genetic disorder caused due to increased levels of phenylalanine in the blood. Untreated, PKU can lead to intellectual disability, behavioral problems, seizures, and mental disorders. This may also cause a bad smell and fair skin. Phenylketonuria is characterized by the absence or deficiency of an enzyme called phenylalanine hydroxylase, responsible for processing the amino acid phenylalanine, an amino acid, a building block of protein. Phenylketonuria is an uncommon but usually dangerous genetic condition. The main phenylketonuria treatment is a low-protein diet that completely avoids high-protein foods (such as eggs, meat, and dairy products) and controls the intake of many other foods, such as cereals and potatoes. It is important to eat a special diet that limits foods containing phenylalanine. This requires close supervision in conju...