Phenylketonuria

The deficiency of dihydropteridine reductase in phenylketonuria leads to imbalances in phenylalanine and other compounds in the body.

Phenylketonuria is a rare disorder that affects the way the body processes phenylalanine.

Early diagnosis and treatment are important for managing phenylketonuria.

Phenylketonuria is an autosomal recessive disorder that results in the accumulation of phenylalanine in the body.

Phenylketonuria is a group of inborn errors of metabolism characterized by defects in tyrosine and phenylalanine metabolism.

Children with phenylketonuria need to follow a strict low-protein diet.

The doctor diagnosed the newborn baby with phenylketonuria.

The support group for families affected by phenylketonuria provided valuable resources and information.