Phenylketonuria is a genetic amino acid metabolism disorder, often inherited in an autosomal recessive manner across generations. When screening results are abnormal, early diagnosis and intervention should be carried out to avoid affecting the child’s growth, development, intelligence, and health. Parents should take their children to the doctor promptly and follow medical instructions for treatment.
Finding the Best Hospital for Phenylketonuria Treatment
Get purchasing advice for specialized Phenylketonuria baby formula
Learn how to purchase special formula milk for babies with Phenylketonuria.
A 45-day-old baby is suffering from phenylketonuria, and the question is whether it can be treated.
Phenylketonuria is a rare genetic disorder that typically manifests in childhood, with adult onset being extremely rare.
Phenylketonuria is a common chromosomal recessive genetic disease with no cure available at present, requiring lifelong treatment.
Mild phenylketonuria (PKU) is a common amino acid metabolism disorder that can be mitigated or prevented from causing brain damage through early diagnosis and long-term dietary control.
After a neonate is diagnosed with phenylketonuria, timely treatment is necessary. Although this genetic disorder is difficult to self-heal, early treatment usually yields better results. However, as the child grows older, treatment may lead to some residual symptoms.
Treatment and Prognosis of Phenylketonuria
